Instrument User Manual - Vitek 2 Compact
Instrument User Manual - Vitek 2 Compact
24410
(09/2009)
bioMérieux, Inc.
Box 15969
Durham, North Carolina 27704-0969 / USA
Tel. (1) 800-682-2666
bioMérieux® SA
EC REP au capital de 12 029 370 €
673 620 399 RCS LYON
69280 Marcy l’Etoile / France
tél. 33 (0)4 78 87 20 00 / fax 33 (0)4 78 87 20 90
http://www.biomerieux.com
[01]
Algeria China Hungary
bioMérieux Algérie EURL bioMérieux China Limited bioMérieux Hungária Kft.
Algéria Business Center Room 1601-02B & 10 Fóto út. 56 (5. emelet)
Les Pins Maritimes - Mohammadia Est Ocean Centre H-1047 Budapest
Alger nº 24A Jiang Guo Men Nei Street tel. (36) 1 231 3050
tel. (213) 21 89 14 81 100004 Beijing fax (36) 1 231 3059
fax (213) 21 89 14 82 tel. (86) 10 6515 6963
fax (86) 10 6515 6993 India
Argentina bioMérieux India Pvt. Ltd
bioMérieux Argentina bioMérieux China Limited A-32, Mohan Co-Operative Ind. Estate
Av. Congreso 1745 Room 2605, South Tower, New Delhi 110 024
C1428BUE World Trade Center tel. (91) 11 42 09 88 00
Capital Federal Buenos Aires 371-375 Huan Shi Dong East Road fax (91) 11 24 64 88 30
tel. (54) 11 5555 6800 510095 Guangzhou
fax (54) 11 5555 6888 tel. (86) 20 8762 7010 Indonesia
fax (86) 20 8762 7015 Representation Office
Australia bioMérieux Indonesia
bioMérieux Australia P/L Colombia Enseval Building
Unit 25 - Parkview Business Centre bioMérieux Colombia Ltda Kawasan Industri Pulo Gadung -
1, Maitland Place Avenida 15 No. 100-43 JI. Pulo - Lentut No. 10
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tel. (61) 2 8852 4700 Bogotá, D.C. tel. (62) 21 461 51 11
fax (61) 2 8852 4777 tel. (57) 1 520 0080 fax (62) 21 460 41 07
fax (57) 1 520 0088
Austria (57) 1 520 0831 Italy
bioMérieux Austria GmbH bioMérieux Italia S.p.A.
Eduard-Kittenberger-Gasse 97 Czech Republic Via Fiume Bianco, 56
Top 3 bioMérieux CZ s.r.o. 00144 Roma
A-1230 Wien Business Park Kosice tel. (39) 06 523 081
tel. (43) 186 50 650 Jinonická 80 fax (39) 06 523 08240
fax (43) 186 50 661 158 00 Praha 5
tel. (420) 2 57 290 623 Ivory Coast
Belgium (420) 2 57 290 232 bioMérieux Afrique Occidentale
bioMérieux Benelux s.a./n.v. fax (420) 2 57 290 964 08 BP 2634
Media Square Avenue Joseph Blohorn
18–19 Place des Carabiniers Denmark Abidjan 08
Bruxelles 1030 bioMérieux Danmark Aps tel. (225) 22 40 93 93/22 40 41 40
tel. (32) 2 743 01 70 Smedeholm 13C fax (225) 22 40 93 94
fax (32) 2 733 55 97 2730 Herlev
tel. (45) 70 10 84 00 Japan
Brazil fax (45) 70 10 84 01 Sysmex bioMérieux, Ltd.
bioMérieux Brasil SA Osaki Central Tower 8F
Estrada Do Mapuá Finland 1-2-2 Osaki Shinagawa-ku
491 Taquara - Jacarepaguá bioMérieux Suomi Oy Tokyo 141-0032
CEP 22710 261 Konalantie 47 C tel. (81) 3 6834 2666
Rio de Janeiro RJ FI-00390 Helsinki fax (81) 3 6834 2667
tel. (55) 21 2444 1400 tel. (358) 9 8545 6000
fax (55) 21 2445 6025 fax (358) 9 8545 6045 Korea
bioMérieux Korea Co., Ltd.
Canada France 1st & 2nd Floor, Yoosung Building
bioMérieux Canada, Inc. bioMérieux SA # 830-67 Yeoksam-dong,
7815, Henri-Bourassa West 69280 Marcy l’Etoile Kangnam-gu
Saint Laurent, QC tel. (33) (0)4 78 87 20 00 Séoul 135-080
H4S 1P7 fax (33) (0)4 78 87 20 90 tel. (82) 2 2188 4700
tel. (1) 514 336 7321 http://www.biomerieux.com fax (82) 2 547 6263
fax (1) 514 807 0015
Germany Mexico
Chile bioMérieux Deutschland GmbH bioMérieux México SA de CV
bioMérieux Chile S.A. Weberstrasse 8 Chihuahua 88, col. Progreso
Seminario 131 D 72622 Nürtingen México 01080, D.F.
Providencia tel. (49) 7022 30070 tel. (52) 55 5481 9550
Santiago fax (49) 7022 36110 fax (52) 55 5616 2245
tel. (56) 2634 20 92
fax (56) 2634 20 93 Greece Netherlands (The)
bioMérieux Hellas S.A. bioMérieux Benelux BV
Papanikoli 70 Boseind 15
15232 Halandri P.O. Box 23
Athens 5280 AA Boxtel
tel. (30) 2 10 81 72 400 tel. (31) 411 65 48 88
fax (30) 2 10 68 00 880 fax (31) 411 65 48 73
New Zealand Singapore Thailand
bioMérieux New Zealand Ltd. bioMérieux Singaporete. Ltd. bioMérieux Thailand Ltd
C/- Logical Freight Solutions 11 Biopolis Way, Helios, Block 11 3195/9 Vibulthani Tower, 4th Floor
12C Rennie Drive, Airport Oaks #10-03 Singapore 138667 Rama IV Road, Klongton, Klongtoey
Auckland tel. (65) 6513 9554 Bangkok 10110
tel. (64) 9 918 6354 fax (65) 6478 9501 tel. (66) 2 661 56 44
fax (64) 9 918 6355 fax (66) 2 661 56 45
South Africa
Norway bioMérieux South Africa Pty Turkey
bioMérieux Norge AS 7 Malibongwe Drive bioMérieux Diagnostik A.S.
Økernveien 145 Randburg 2125 Değirmen Sok. Nida Plaza Kat:6
N-0513, Oslo tel. (27) 11 801 91 10 34742 Kozyataği-Istanbul
tel. (47) 23 37 55 50 fax (27) 11 791 24 19 tel. (90) 216 444 00 83
fax (47) 23 37 55 51 fax (90) 216 373 16 63
Spain
Philippines (The) bioMérieux España S.A. United Kingdom
Representation Office Manual Tovar, 45–47 bioMérieux UK Ltd
bioMérieux Philippines 28034 Madrid Grafton Way, Basingstoke
11th Floor, Pearlbank Centre tel. (34) 91 358 11 42 Hampshire RG22 6HY
146 Valero Street, Salcedo Village fax (34) 91 358 06 29 tel. (44) 1256 461881
1227 Makati City fax (44) 1256 816863
tel. (632) 817 7741 Sweden
fax (632) 812 0896 bioMérieux Sverige AB USA
Hantverksvägen 15 bioMérieux, Inc.
Poland 436 33 Askim 100 Rodolphe Street
bioMérieux Polska Sp. Z.o.o. tel. (46) 31 68 84 90 Durham NC 27712
Ul. Zeromskiego 17 fax (46) 31 68 48 48 tel. (1) 919 620 2000
01-882 Warsaw
tel. (48) 22 569 85 00 Switzerland Vietnam
fax (48) 22 569 85 54 bioMérieux Suisse s.a. Representation Office
51, avenue Blanc bioMérieux Vietnam
Portugal Case postale 2150 Room 4A, 4th Floor
bioMérieux Portugal, Lda. 1211 Genève 2 Green House Building
Av. 25 de Abril de 1974, nº 23-3º tel. (41) 22 906 57 60 62A Pham Ngoc Thach Street, Ward 6
2795-197 LINDA-A-VELHA fax (41) 22 906 57 42 District 3
tel. (351) 21 415 23 50 Ho Chi Minh City
fax (351) 21 418 32 67 Taiwan tel. (84) 88 209 906
Representation Office fax (84) 88 209 905
Russia bioMérieux China Limited
o.o.o. bioMérieux Taiwan Branch
Derbenevskaya ul. 20, str. 11 RM 608, No. 6-3 Ching Cheng Street
115 114 Moscow Taipei 105
tel. (7) 495 221 10 79 tel. (886) 2 2545 2250
fax (7) 495 221 10 79 fax (886) 2 2545 0959
Liability Disclaimer
Intellectual Property
Seller shall not be liable under this Warranty for any defect arising from
abuse of the system, failure to operate and maintain the system in
accordance with the documentation included with the Instrument, including
repair service, alteration or modification of the system by any person other
than service personnel of bioMérieux, Inc., or use of modified, changed, or
previously used disposables.
The warranty of Seller set forth above and the obligations and liabilities
of Seller thereunder are exclusive and in lieu of all other remedies or
warranties, express or implied, arising by law or otherwise, with respect
to the system delivered hereunder (including without limitation any
obligation of Seller with respect to merchantability, fitness for particular
purpose and non-infringement). In no event shall Seller be liable for
incidental or consequential damages, however arising and whether or
not occasioned by Seller’s negligence.
All of the product elements in the Seller’s Instrument and the total
Instrument are warranted to be new or equivalent to new for the full product
warranty period of one year. Disposables and replacement items with a
normal life expectancy of less than one (1) year, such as batteries and bulbs,
are excluded from this warranty.
TABLE OF CONTENTS
CONFIGURATION........................................................................................................................3-1
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
Chapter Contents. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
Configuration Options. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Setting Configuration Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Configuration Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Instrument Name . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
Setting Instrument Name . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Date Format . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Setting Date Format . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Schedule QC Status. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
QC Status . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-8
Alert Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
Alert Categories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
Setting Alert Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-10
Alert Volumes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-11
Setting Alert Volumes Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-11
Display Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-12
LCD Screen Contrast . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-12
Keyclick Volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13
Setting Range Values. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-14
APPENDIX C ..............................................................................................................................C-1
Instrument Error Code User Response Table . . . . . . . . . . . . . . . . . . . . . . . . . . . C-1
Using the Error Code User Response Table . . . . . . . . . . . . . . . . . . . . . . . . . C-1
Cycling the Power of the Instrument . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-1
IMPORTANT: Read this manual carefully before attempting to operate the VITEK® 2
Compact system.
Note: The instrument conforms to the relevant European regulations for electrical
safety and EMC.
Chapter Contents
The software provided with the VITEK® 2 Compact system includes analysis
and data-management programs. A bidirectional computer interface
transfers results automatically to the user’s laboratory information system
(LIS) and to various product and patient reports.
This manual focuses on the VITEK® 2 Compact instrument and how to use it
in the user’s workflow. It contains step-by-step procedures for using the
instrument.
Note: The computer, printer, dispenser, and DENSICHECK are packaged with their
own instructions for use and maintenance.
By using the information and procedures in this manual, the user can
perform all the functions required to operate the system, including:
For more information on test cards, see the VITEK® 2 Compact Online
Product Information. For more information on software workflow and
procedures, see the VITEK® 2 Compact Online Software User Manual.
Note: Screens and figures are intended for illustrative purposes only and are not
to be construed as representations of actual test data, results, or
components. Screens and components are not shown to scale.
Additional Supplies
Contact bioMérieux or the local vendor for laboratory supplies and other
accessories.
Intended Audience
The VITEK® 2 Compact system and this manual are intended for laboratory
use by trained, professional, clinical and industrial users. Most material in the
manual applies to both sets of users.
Note: If any information in the manual is intended for clinical use only or industrial
use only, it is marked Clinical Use or Industrial Use.
Manual Organization
Chapter Organization
All of the workflow and procedural chapters are organized in the same way
and include the following:
• Procedures
Finding Topics
This manual uses several methods to help you find information and keep
your bearings:
Table of Contents — Located at the front of the manual. It contains the titles
of all chapters/appendices and their sections, and the page number of each
title and section.
List of Figures — Located at the front of the manual. It contains a list of all
figures in the manual and the page number of each figure.
List of Tables — Located at the front of the manual. It contains a list of all
tables in the manual and the page number of each table.
Chapter Contents — Located at the front of each chapter. It lists all sections
in the chapter and their page numbers.
Page Headers — Located at the top of each page. There are two parts to a
header: the chapter title and the primary section title.
Page Footers — Located at the bottom of each page. There are four parts to
a footer: the manual’s title, the manual’s part number, the revision date (if
applicable), and the page number.
Index — Located at the back of the manual. It contains topical entries and
their page numbers.
The names of windows and screens are in Proper Case, but are not bolded.
Press
This manual uses the word “press” to refer to pressing a key on the user
interface in order to initiate action in the firmware.
We also use the word “press” to refer to pressing switches and buttons on
the instrument or other hardware components.
Procedural Steps
Steps in procedures are sequentially numbered. A bullet list in a step
indicates options.
References
References to chapter and section titles in this manual are in Proper Case.
Select
The word “select” is generally used for selecting menu commands and for
user interface navigation.
User Input
Instructions for user input begin with the word “type” or “enter.” This manual
uses bold for literal user input and italic for placeholders.
In this example, you are to type exactly what you see on the page (April 1 in
this example).
WARNING
Warning is a statement that alerts the user to the possibility of
injury, death, or other serious adverse reactions associated with
the use or misuse of a device.
Standard Symbols
The following table presents symbols that may appear in the instructions
for use or on the instrument, package inserts, or packaging.
CE-Marking of Conformity
Use by
Manufacturer
Date of manufacture
Keep dry
Biological risks
Radiation warning
Laser
Temperature limitation
Batch code
Catalog number
Serial Number
Do not reuse
Recyclable
Very toxic
Corrosive
Sodium azide
Irritant
Positive control
Negative control
This way up
Do not stack
Humidity limitation
Fuse
Direct current
Alternating current
Equipotentiality
ON (supply)
OFF (supply)
Chapter Contents
Installation Recommendations
WARNING
Due to the nature of the instrument, the potential exists for
personal injury or damage to the instrument from electrostatic
discharge.
Access Doors
Figure 2-1 illustrates the location of instrument access doors.
2
1
5 4
2 — Front User Access Door. Provides access to the optics, incubator, and a
portion of the test card transport system.
3 — Top User Access Door. Opens only when the Front User Access Door is
open, and provides access to the optics and carousel. This door lifts from the
front (Figure 2-3) and remains in the open position until the operator closes
it.
Locking mechanisms prevent the Load Door and Front User Access Door
from opening during operation. The Top User Access Door is not equipped
with its own lock, but it cannot be opened when the Front User Access Door
is locked.
7 — Door Latch and Lock. The latch holds the door closed, while the locking
mechanism consists of a pin extending from inside the cabinet into the latch,
locking the door.
Figures 2-3 and 2-4 show the instrument with the doors open.
10 9
Figure 2-4: Fill Door, Load Door, and Waste Collection Door Open
8 — Filler Station
1 — User Interface Screen and Keypad. This screen and keypad comprise
the instrument User Interface system.
2 — Fill Indicator LED. Alerts user of the fill status. See Table 2-2 on
page 2-11.
Connections
This section illustrates the exterior connections located on the VITEK® 2
Compact instrument.
1 — UPS Connection. Located on the left side of the instrument. This cable
connector port connects the instrument to an optional uninterruptible
power supply (UPS). Through this port, the UPS notifies the instrument of a
power failure, so it can begin appropriate procedures.
Startup Procedure
1) Make sure the instrument is connected to an appropriate power supply
using the power cord supplied with the instrument.
After a few minutes, the Status screen appears. The Status field at the
bottom of the screen (Figure 2-10) should show a status of Warming or OK.
The Warming status means that the carousel temperature is not yet within its
specified range. This typically takes 5 to 15 minutes.
VITEK® 2 Compact is ready to begin processing cards when the Status field
displays OK.
Internal Processing
Test Card Incubation and Reading Test card analysis page 2-15
The Cassettes
The cassette is the main component of the test card transport system. It can
hold up to 10 test cards with their inoculum test tubes.
WARNING
The cassette should be considered as potentially contaminated
and should be handled appropriately. Qualified laboratory
personnel should take the usual precautions necessary for
handling infectious agents. Extreme caution should be
exercised when handling broken test tubes.
Test Card Slots. The top portion of a cassette is divided into 10 test card
slots that can hold various combinations of VITEK® 2 Systems test cards.
Test Tube Holders. The cassette has 10 wells that hold test tubes for
inoculum.
Cassette Base. The base of a cassette is custom shaped to fit into the Filler
and the Cassette Load/Unload stations and is designed with a hand grip
located on the end of the cassette opposite the bar code.
Cassette Bar Code ID. Located on the front side of the cassette. This bar
code identifies the cassette to the instrument.
Filler Station
The station consists of the fill door, fill chamber, and an indicator LED. At the
Filler (vacuum) station, all of the test cards in a cassette are inoculated with
the suspension contained in their corresponding test tubes.
For fill indicator status descriptions see Table 2-2 for details.
Note: Clean the filler seal periodically. See Chapter 5 for maintenance details.
The Filler Station uses a vacuum chamber and pump. When the cassette is
placed in this station, the operator initiates the filling cycle by closing the
door and pressing the Start Fill button. The following steps occur:
1) The pump evacuates the air from the chamber. This forces the air inside
each test card to escape via the transfer tube and bubble up through the
suspension. The channels and wells inside of each test card are now at a
vacuum.
2) After a short period, the instrument slowly releases the vacuum. The
increasing air pressure inside the chamber forces the suspension in each
test tube through the transfer tube and into the channels and wells of
the test card.
Various temperature and air pressure sensors in the system monitor the
inside of the vacuum chamber. VITEK® 2 Compact ensures proper test card
fills by monitoring these parameters throughout the entire cycle and
controlling the rate at which the vacuum is drawn and released.
Solid Blue Arrow Cards are processing in the station and the cassette load
door is locked and cannot be opened.
Blue Blinking Arrow The cassette is ready to be removed from the station. The
cassette load door is unlocked. When you remove the
cassette and close the door, the indicator LED turns off.
3
Figure 2-16: Bar Code Reader
1 — Bar Codes
2 — Bar Code Scanner
3 — Beam
• Test card lot information and sequence number. This includes the test
card’s lot number to provide manufacturing traceability. The sequence
number uniquely identifies a test card.
In addition to reading the bar codes on the cards, the reader also scans the
bar code located on the cassette itself. This bar code identifies the cassette
to the instrument as cassette one through nine.
Note: The bar code reader inside the instrument has no lasers and is certified to
IEC60825-1 LED Safety: Class 1.
Sealer Station
A heated wire comes in contact with each transfer tube. The plastic tube
melts, causing most of it to separate from the test card and drop into the test
tube. The portion that remains attached to the test card is sealed by the
melting plastic. The instrument produces small amounts of fumes during
sealing, which is normal and non-toxic.
Note: The sealer leaves a stub that remains from the transfer tube. The stub may
be up to 0.06 inch (1.5 mm) long and does not affect normal operations.
Carousel
The Incubator (Figure 2-17) with the cover in place, contains a Carousel with
a capacity of 15 to 60 test cards depending on the option purchased. During
their time in the carousel, the test cards are incubated at an average
temperature of 35.5 °C.
Note: Figure 2-17 is shown with the optional thermometer (black disc). This
thermometer can be independently calibrated to NIST traceable standards
and offers a method of checking temperature independent from the internal
devices. Instructions for use of this instrument are included in Chapter 5.
Figure 2-18 depicts the carousel inside the incubator without the cover.
As the carousel rotates, each test card moves into the reading position every
15 minutes. The reader head conveys the test card through the optics
stations then back to the carousel, where it continues to incubate until its
next read cycle. After the reading cycles are completed, the instrument ejects
the cards into the waste collection station.
Note: The carousel is divided into four sections so that it can be easily removed for
periodic cleaning. See Cleaning the Carousel in Chapter 5.
Transmittance Optics
VITEK® 2 Compact performs its identification and susceptibility analyses by
continually monitoring the growth and activity of organisms inside the wells
of the test cards.
The optics use light emitting diodes (LEDs), which produce light at the
appropriate wavelengths, and silicon photodetectors to capture the
transmitted light. This system is self-calibrating.
Note: Clean the optics periodically. See Cleaning the Optics (With Cards
Processing — Power On) and Cleaning the Optics (Power Off) in Chapter 5
for further details.
Card Ejection
The card ejection function permanently removes test cards from the carousel
after their testing is complete or deleted/terminated by the user. The
mechanism that performs this function is the same drive belt system that
moves the test cards through the reader. Instead of returning to the carousel,
an ejected test card continues on to the waste collection station.
The amount of time that cards are held before being ejected automatically
from the carousel is set by an option in the System Configuration window at
the workstation computer. You can also eject test cards at any time using the
manual ejection function. See the VITEK® 2 Compact Online Software User
Manual for details regarding this function.
The waste collection bin (Figure 2-20) holds up to 60 test cards. The
instrument counts test cards as they fill the bin, and sends a message to the
instrument interface screen when the station is full. A sensor in the station
detects when the bin is emptied or if the bin is missing.
IMPORTANT: Do not remove the waste collection bin without disposing of the cards.
The instrument assumes cards are emptied from the waste collection
bin when it detects the bin is missing then replaced.
Access the Waste Collection station by opening the waste collection door on
the front of the instrument. Keep the waste collection station door closed
except when removing test cards from the station.
Periodically remove the waste collection bin for cleaning. See Cleaning the
Waste Collection Bin in Chapter 5.
3 — Status/Menu Key. Use this key to select either the Status screen or
Menu screen or to access the Status screen from any screen.
5 — Message Key. Press this key at any time to access the Error Message
queue. This key is also used to go between the Detailed Error Messages and
List of Error Messages screens.
Note: When Arrow keys are active, their icons appear on the display.
Menu System
All of the functions used on the VITEK® 2 Compact instrument are available
through the menu system. The system is composed of a Main menu and a
set of five submenus.
Figure 2-23 depicts the menu structure with all of the function options
added. The lines show the menus and the pathways between them.
Incubator
Remove Carousel Cabinet Date Format
System Number
Optics Cleaning Alert Options
Serial Number
Alert Volumes
Last Maintenance Date
All
Optics Self Test Fill Complete
Cassette Success
Cassette Exception
Sub-system Error Status
Intervention
Error in Queue
Display Options
2-21
Menu System
Menu System Instrument Overview
Chapter Contents
Configuration Options
There are six configuration options and 18 sub-menu options, all of which
you access through the instrument Main menu on the VITEK® 2 Compact
user interface. Use these options to set basic operating parameters such as
system name and date format.
2) Evaluate the effect that an option would have on your workflow and
decide how to set the option.
3) Set the options according to the choices made in step 2. Use the
procedures in this chapter to set an option.
Configuration Menu
All configuration options for VITEK® 2 Compact are located on the
instrument Configuration menu.
1) Press the Status/Menu key from the Status Screen to access the Main
menu screen. The following screen displays.
Instrument Name
1 — Key is non-functional
2 — Key is non-functional
3 — Deletes all characters
4 — Backspace Key
5 — Insert Key
1) Press the Status/Menu key from the Status Screen to access the Main
menu screen.
4) Select Clear to ensure that the field is ready to accept new characters.
5) Select a letter using the Arrow keys and then press the Insert key for the
character box. If you make a mistake, press the Backspace key.
The instrument automatically saves the Instrument Name when you leave
the Instrument Name screen by pressing the Previous Screen, Status/
Menu, or the Message key.
Date Format
Use the date format option to configure how the date appears (for example,
MM/DD/YY or YYYY/MM/DD).
To access the Date Format screen:
1) Press the Status/Menu key from the Status Screen to access the Main
menu screen.
The instrument automatically saves this format when you exit the screen by
pressing the Previous Screen, Status/Menu, or Message key.
Schedule QC Status
By using the QC Status from the main menu, you can manually record a QC
Status at any time. See QC Status on page 3-8 for further information.
You can also schedule up to three times a day for the system to record a QC
Status report.
After the instrument records the QC Status, it sends the information to the
workstation computer, which records the data along with the date and time
the data was recorded.
The time fields operate on a 24-hour clock. The times for Schedule A, B, or C
are disabled until you schedule the QC Status.
1) Press the Status/Menu key from the Status Screen to access the Main
menu screen.
Note: To disable any schedule, follow steps one, two and three in this section and
select DISABLE.
4) Use the Number keys to set the hour, then the minutes.
5) Press the Accept key to save the time and return to the previous screen.
7) To exit the Schedule QC Status screen, press the Previous Screen key or
Status/Menu key.
Note: If you enter an incomplete schedule (i.e., you entered the hour, but not the
minute), the system restores the previous schedule, but does not save the
new schedule. An error message appears on the first screen (Figure 3-8).
The instrument automatically saves the schedule when the user leaves the
second screen by pressing the Previous Screen, Status/Menu, or Message
key.
QC Status
This function is used to view the current status report of the incubator
temperature and the optics (Figure 3-9). This report can be manually sent to
the workstation PC at any time.
Last report recorded on: Displays the date and time that the previous QC
Status was recorded.
Note: The Previous Screen key or Status/Menu key can also be used to exit from
QC Status.
Alert Options
The instrument gives an audible and/or visual alarm to alert you to an error
condition or warning. There are several categories of alarms.
Audible Indicator
Blink Indicator
Alert Categories
You can customize individual alert categories. An intervention, for example,
might be set at a high volume, so the user knows attention is required.
• All – All of the categories use the same alert option or alert volume.
• Error in Queue – New errors are present in the Error Message Queue.
• Load Timeout Warning – Cassette load timeout warning; less than one
minute remaining to transfer the cassette from the Filler Station. to the
Cassette Load/Unload Station.
1) Press the Status/Menu key from the Status Screen to access the Main
menu screen.
2) Select Configuration.
4) The Alert Options screen appears (Figure 3-11). Use the Up/Down
Arrow keys to view additional categories.
5) Select a category using the Function keys. Three options display on the
next screen. The X mark indicates the current alert option.
6) The instrument automatically saves this option when you exit the screen
by pressing the Previous Screen, Status/Menu, or Message key.
Alert Volumes
Use the Function keys to select a category for volume configuration. The
default setting for the alarm volume is at a comfortable level. Use this option
to make appropriate adjustments as required.
1) Press the Status/Menu key from the Status Screen to access the Main
menu screen.
2) Select Configuration.
3) Select Alert Volumes from the Configuration menu.
4) The Alert Volumes screen appears (Figure 3-12). Use the Up/Down
Arrow keys to view additional categories.
Whenever the right or left arrow is pressed, the system sounds the alert at
the selected volume.
If you select the Blink Only option for a category, the system displays a
warning message (Figure 3-13). However, the user can still set the volume.
The instrument automatically saves the configuration when you leave this
menu screen by pressing Previous Screen, Status/Menu, or Message key.
Display Options
The VITEK® 2 Compact user interface screen uses an LCD display. You can
control the amount of background contrast on the display by configuring the
Display Options.
Keyclick Volume
The VITEK® 2 Compact instrument interface uses a touchpad type of keypad.
It sounds an audible click when you press each key. You can adjust the
volume of the click to account for laboratory conditions.
You can set Range Values for the following configuration options:
2) Change the range value by pressing the Left/Right Arrow keys. The bar
graph and the numeric value change, and the actual parameter changes
in response to this action.
This chapter contains the procedures you need to process test cards. The
chapter begins with introductory sections that provide reference information
about the VITEK® 2 Compact Status screen and the VITEK® 2 Compact menu
system.
The following sections contain suggested workflow and procedures. The final
section describes how to unload test cards from the instrument.
Chapter Contents
The Status screen is used more often than any other screen in the VITEK® 2
Compact user interface. Since it is basic to the workflow, the Status screen is
easy to display and, in many cases, the interface displays it automatically.
This section details the various icons and informational messages that you
see while operating the instrument.
• Press the Status/Menu or Previous Screen key from the Main menu.
• Press the Status/Menu from any menu or error message queue screen.
The Status field appears at the bottom of the VITEK® 2 Compact Status
screen.
The white section at the bottom of the screen may contain three types of
information:
1) New Error/Warning Indicator (!). See New Error/Warning Indicator on
page 4-9.
3) Current Time of the day in 24-hour format. This time is based on Host/
Workstation Computer time (for example, 10:35).
• Warming. This status displays after instrument startup or any time the
incubation temperature in the reader station has not reached its specified
temperature. The instrument can still process cards when the status
Warming is active.
Filler Status
The Filler Status includes a Filler Status indicator on the left and a possible
Detailed Message/Action on the right. If there are any warnings or errors
related to filling the cards, an Intervention screen appears.
Idle
When the display reads Filler: Idle, the instrument is ready to start the fill
cycle.
The Start Fill function is shown on the upper-right side of the screen. Press
the Start Fill key to initiate the fill cycle.
Filling
The screen displays Filler: Filling when the filling process has started. The
Filling-in-progress indicator displays (Figure 4-3) to indicate filling.
This indicator overwrites the Start Fill box, and tells the user the cards are
filling; it does not show the actual progress or stage of the filling cycle. When
the entire bar is filled, it repeats from the beginning until the fill cycle is
complete.
Complete
The Filler: Complete indicator shows that the fill cycle is done, and the
cassette is ready for transfer into the Loader. This Filler: Complete indicator
displays regardless of fill success or failure, and the instrument provides an
alert to indicate that the fill is complete. This alert can be audible and/or
blinking, depending on the custom settings.
Not Ready
When the Filler: Not Ready indicator displays, the instrument cannot start
the filling cycle, because either the Filler is not ready or there is a fault
condition in the Filler or in the instrument.
WARNING
Biohazardous spills can occur inside the VITEK® 2 Compact
instrument. All organism suspensions should be considered as
potentially infectious.
Loader Status
The Loader Status sub-screen is comprised of two parts: Loader Status on
the left and a display area for messages on the immediate right. Based on
the workflow, under error-free conditions, the Loader Status proceeds as
follows:
Empty Status > Transfer Cassette > Bar Code Reading > Sealing >
Loading into Carousel > Remove Cassette
Empty Status
When there is no status in the Loader field, the loader is not ready for the
user to load a cassette, and the loader door is locked.
Transfer
When the Loader: Transfer message displays, the filling cycle is complete
and the user should transfer the cassette from the Filler Station to the Loader
station. A maximum of 10 minutes is allowed to transfer the cassette. After
this time period, the system no longer accepts the cards. This countdown is
visible in the upper-right corner of the screen.
The instrument provides an alert for Cassette Success, if the cassette setup
is OK, as well as a unique alert for Cassette Exception if the cassette setup
has non-correctable errors.
Sealing
The Loader: Sealing message indicates that the instrument successfully read
the bar codes, and the instrument continues to process the card cassette for
sealing.
Loading Card
The Loader: Loading Card message means that the sealing is complete, and
the instrument is loading cards into the carousel.
Remove
When Loader: Remove message displays, the instrument has finished
processing the cards in the cassette, and the cassette is ready for the user to
remove. However, if there are still cards remaining in the cassette, an error
condition has occurred and the user was not able to fix the error.
Cassette Number
The icon to the right of the Loader Status displays after successful bar code
reading and the cassette number is known.
Countdown Timer
A countdown timer in the upper, right corner of any screen displays in the
Start Fill area and indicates the total number of minutes and seconds left for
the user to transfer the cassette from the Filler to the Loader. The
continuation of this counter is used when any other Intervention Message
displays.
General Status
The General Status portion of the screen uses various icons to display
messages that alert the user to these general conditions. Users should
become familiar with these indicators to ensure smooth operation of the
instrument.
Note: Some of these indicators or icons are only visible on the screen when the
function they represent is active.
UPS Status
UPS is present, and there is a power failure.
UPS Battery
UPS is present, and the battery is low.
Instrument Name
The name of the instrument as input by the user.
Available Slots
This icon indicates the number of available slots in the carousel. The number
range is zero to 15, zero to 30, or zero to 60 depending on the instrument
model.
The Available Slots field indicates the number of unoccupied slots in the
instrument. You can load one or more cassettes containing up to that
number of test cards. If you load more than that number, the instrument will
not process some of the test cards unless additional slots become available
by the time the test cards reach the carousel.
Cassette Presence
The cassette is present in the Loader Station.
user has not viewed. This indicator moves from side to side on the screen.
The instrument sounds an alert and/or the screen blinks (depending on the
configuration settings), if there is an error or warning in the queue. Press the
Message Key (!) to view the Error Message Queue. The screen below
displays the message queue indicator’s warning icon (bottom left).
For more information, refer to the VITEK® 2 Compact Online Software User
Manual.
• Setup Tests Post Entry (Cassette Only Mode). The user loads the
cassette into the instrument prior to entering the cassette information into
the workstation computer.
The Workflow
The following table provides a generalized workflow for working with the
VITEK® 2 Compact instrument.
Table 4-1: Workflow
Activity Reference
3) Fill in the cassette worksheet with the Cassette Preparation on page 4-12.
test card and specimen information for See VITEK® 2 Compact Online
the cassette. Software User Manual for additional
details.
4) Place the test cards and specimen test See VITEK® 2 Compact Online
tubes in their appropriate slots. Software User Manual for additional
details.
6) Load the cassette into the Filler Station. Filler Station on page 4-13.
8) If the cassette bar code was not read and Cassette Preparation on page 4-12.
performed on the user interface screen of See VITEK® 2 Compact Online
VITEK® 2 Compact, access the Manage Software User Manual for additional
Cassette view function on the VITEK® 2 details.
Compact workstation. Enter a cassette
number.
9) If using the Setup Tests Post Entry The VITEK® 2 Compact Online
method, enter the information from the Software User Manual.
cassette worksheet into the Setup Tests
Post Entry.
Cassette Preparation
Follow these procedures to set up the test cards and specimens for a
cassette.
During the first minute after you load a cassette, the instrument reads the
bar code on each test card. From this bar code reading, the instrument
knows the number of test cards in the cassette, the type of test cards, and
the position of each test card. The instrument sends this information, along
with the cassette number read during the bar code reading process, to the
workstation.
You can view this information in the Setup Tests Post Entry window, which is
part of the VITEK® 2 Compact workstation software. You can access the
window and, using the Cassette Worksheet, fill in the remaining information
for the cassette after you load the test cards into the carousel.
For information on using the Setup Tests Post Entry window, refer to the
online VITEK® 2 Compact Online Software User Manual.
WARNING
Biohazardous spills can occur inside the VITEK® 2 Compact
instrument. All organism suspensions, cards, cassettes, test
tubes, sample transfer tubes, waste bin and the user interface
panel should be considered as potentially infectious.
Before you load the cassette into the Filler Station, check the Status screen.
Look at the following parameters to make sure it is OK to start a fill.
Available Slots The value in this field should be greater than or equal to
the number of test cards you are loading.
Filler Station
The Filler Station consists of the fill door, fill chamber, and an indicator LED
(Figure 4-5). This indicator displays the status of the Filler Station. See table
2-3 for a description of the Load Indicator Status.
After loading cards and inoculum into the cassette, place the cassette in the
Filler Station. When you press the Start Fill key, a vacuum pump evacuates
the air from the chamber. When the instrument releases the vacuum, the
pressure of the air replacing the vacuum forces the samples to flow into and
inoculate the test cards.
4) After completion of the Fill cycle (the Fill indicator’s blue LED blinks),
remove the cassette from the Filler Station and close the Fill door.
Loading a Cassette
WARNING
The cassette should be considered as potentially contaminated
and should be handled appropriately. Qualified laboratory
personnel should take the usual precautions necessary for
infectious agents.
1) Open the Fill door and remove the cassette. The Load door unlocks.
2) Open the Load door and place the cassette into the Cassette Load/
Unload Station.
3) Close the Load door. The cassette icon appears on the Status screen.
Note: It is recommended that the user monitor the process until all the cards are
scanned by the bar code reader. The process is completed when the
instrument sounds the Cassette Success or Cassette Exception alert.
Unloading a Cassette
Unload a Cassette
During test card processing, the instrument unloads the test cards from the
cassette and places them into the carousel.
When the cassette returns to the Load Station, only the specimen test tubes
and the severed transfer tubes remain in the cassette. You must remove the
cassette, so that the station is available to accept another cassette.
1) When you are processing test cards, a blinking, blue indicator LED at the
Load station indicates that an empty cassette is at the station. A red X
indicator signals an error has occurred and user intervention is
necessary.
2) Open the Load door and remove the cassette from the instrument.
4) Dispose of the materials in the cassette. You can now use the cassette
to process additional test cards.
WARNING
All of the materials in an empty cassette should be treated as
biohazards and disposed of accordingly. All organism
suspensions should be considered as potentially infectious.
Qualified laboratory personnel should use acceptable
procedures for biohazardous material.
Remove ejected test cards routinely to ensure that VITEK® 2 Compact can
continue to support your laboratory’s workload.
When the instrument ejects a test card, it removes the card from the
carousel/incubator to the Card Reader and places it in the Waste Collection
station (Figure 4-8). The bin has a capacity of 60 test cards. However, we
recommend that you check and empty the waste bin before it reaches
capacity.
2) Remove the Waste Collection Bin from the station by pulling the front
edge of the bin toward you.
Note: The instrument resets the waste count only if the bin is completely removed.
WARNING
Although VITEK® 2 Compact test cards are sealed, they should
be treated as biohazards and disposed of accordingly.
Note: If the waste collection bin is not replaced, the instrument cannot eject cards.
WARNING
User should not attempt to gain entry into the power supply
area at the rear of the instrument. A possible shock hazard
could exist.
Chapter Contents
This is the first option in the Maintenance menu and is a manual override of
the locking system. Use caution when selecting this option. Cards will not
process when the User Access Doors are open.
Note: When cards are incubating and this option is selected, a confirmation screen
appears to confirm pausing the card processing.
2) A message appears asking the user to confirm unlocking the User Access
Doors.
Note: If the cassette is processing in the Filler Station or in the Cassette Load/
Unload Station the user is not able to unlock the door.
4) When the Front User Access Door is unlocked, both User Access Doors
can be opened.
• More than one hour has passed from the time of power up.
• More than one hour has passed after cards were loaded into the carousel.
Note: If the cassette is processing in the Filler Station or in the Cassette Load/
Unload Station, the user is not able to check the temperature.
4) When the Front User Access Door is unlocked, both User Access Doors
can be opened to check the temperature.
6) Clip the thermometer into place on the white plastic clip. (Figure 5-2).
7) Remove the thermometer by lifting the clip and gently pulling it straight
out of the cover. You may also leave the thermometer in place.
8) Check the temperature and close the User Access Doors when you are
done.
WARNING
The carousel should be considered as potentially contaminated
and should be handled appropriately. Qualified laboratory
personnel should take the usual precautions necessary for
infectious agents.
WARNING
Elevated Temperatures. Do not touch the metallic incubator
venting plate (located behind the carousel sections).
WARNING
Do not put your hands in the carousel when the carousel is
rotating, otherwise an injury could occur.
Note: If there are cards processing anywhere in the instrument, a screen prompts
you to make sure processing is complete and all cards were ejected from the
instrument before cleaning.
If cards are not processing in the incubator, and the carousel sections were
not removed, the following screen displays and the Front User Access Door
unlocks.
CAUTION: Do not open the User Access Doors and remove the
cover as soon as ‘Yes’ is selected. The carousel has moving parts
that are rotating into position. Wait until the carousel stops
moving.
IMPORTANT: If you press the Yes function key, you must remove all of the sections.
This requires about four minutes. Selecting No is the only opportunity to
cancel this operation.
Followed by:
4) When the screen displays Remove Section 1, open the Front User
Access Door.
6) Remove the carousel cover from the carousel by lifting the top of the
cover straight up from the instrument.
Note: Once the carousel is moved to the correct position, the message on the
screen changes (Figure 5-9).
7) Grasp the first carousel section and tilt it to the left, then toward you.
8) Press the Done function key to confirm removal of the carousel section.
The following screen appears.
The carousel turns so you can remove the next section. During this time
the message Preparing for Section Removal displays again on the
screen.
9) Repeat this procedure until all four carousel sections are removed. The
following screen appears.
10) Carefully replace the carousel cover over the carousel and close the User
Access Doors.
11) After the four carousel sections are removed, the Maintenance menu
appears.
For instructions on replacing the carousel, see the section Replacing the
Carousel.
• 5% bleach solution
Note: To disinfect a contaminated surface, use a 10% bleach solution and allow it
to remain in contact with the contaminated surface for five minutes.
4) Take any one of the carousel sections and orient it (Figure 5-14). The
bottom of the section should touch the base plate and the top portion
should tilt slightly toward the left of the instrument. Align the notch to
the spring-loaded pin for the correct locking position.
5) Slide the section down along the base plate while maintaining the tilted
angle.
6) When the section is pushed down all the way, release the top portion,
allowing it to rest against the base plate. Two pins on the back of the
section should engage the two holes in the base plate and secure the
section.
8) The carousel turns 90° to move the first section out of the way. During
this time, the message Rotating Carousel: Please Wait displays on the
screen.
9) Repeat this procedure until all four carousel sections are replaced.
10) Replace the carousel cover over the carousel. If this is not replaced, a
jam condition intervention occurs.
Note: The Front User Access Door does not latch unless the Top User Access Door
is closed.
WARNING
The cassettes should be considered as potentially contaminated
and should be handled appropriately. Qualified laboratory
personnel should take the usual precautions necessary for
infectious agents.
• 5% bleach solution
Note: To disinfect a contaminated surface, use a 10% bleach solution, and allow it
to remain in contact with the contaminated surface for five minutes.
Instrument Shutdown
It is recommended that you shut down the instrument and turn the power
OFF during some of the maintenance procedures. The remaining cleaning
processes described in this chapter require the power to be turned OFF.
Always use the shut-down function from the user interface to turn off the
instrument.
You may clean the following components with the instrument’s power still
on:
• cassettes
• waste collection bin
• filler station
• optics
If any cards are processing, the instrument displays the following screen:
When this process is complete, the instrument displays the message Ready
for Shutdown.
WARNING
Electric shock hazard. Always turn the instrument OFF prior to
removing the power cord.
Note: bioMérieux recommends that you shut down and power OFF the instrument
during this maintenance procedure.
After performing the procedure for instrument shutdown, follow these steps
to clean the optics.
2) Lift the Top User Access Door. This exposes the transmittance optics, as
shown in the following figure.
The transmittance optics consist of two modules that are hinged on the
bottom and held in place by spring-loaded levers.
3) Using your right hand, grasp the module units and place your thumb on
the levers (Figure 5-21). Both optics units must be released
simultaneously to rotate down for cleaning.
4) Push down on the levers to release both units and rotate downward.
7) Rotate the units back into place while pushing down slightly on the
lever. The units click into place when secured.
If you are not performing the remaining cleaning procedures in this section
and the instrument is already turned off, go to the procedure Turning the
Instrument On on page 5-21.
WARNING
Biohazardous materials could come in contact with the exterior
of the VITEK® 2 Compact instrument. All organism suspensions,
cards, cassettes, test tubes, sample transfer tubes, waste bin
and the user interface panel should be considered as potentially
infectious.
Note: bioMérieux recommends that you shut down and power OFF the instrument
during this maintenance procedure.
• 5% bleach
1) Dampen a cloth with one of these approved solutions and wipe off any
dust or dirt from the top, front, and side surfaces of the instrument. Wipe
off all User Access Doors.
Note: To disinfect a contaminated surface, use a 10% bleach solution and allow it
to remain in contact with the contaminated surface for five minutes.
2) Dampen a separate cloth with plain water and wipe the surface again to
remove any disinfectant residue.
WARNING
Do not liberally apply liquid to the exterior surface of the
instrument, display, or keypad. Ingress of liquid could result in
loss of instrument function or a shock hazard.
Note: bioMérieux recommends that you shut down and power OFF the instrument
during this maintenance procedure.
WARNING
Biohazardous materials could come in contact with the interior
of the VITEK® 2 Compact instrument. All organism suspensions,
cards, cassettes, test tubes, sample transfer tubes, and waste
bin should be considered as potentially infectious.
2) Thoroughly clean and dry the bin before replacing it in the VITEK® 2
Compact instrument.
• 5% bleach solution
Note: To disinfect a contaminated surface, use a 10% bleach solution and allow it
to remain in contact with the contaminated surface for five minutes. Using
plain water, wipe the surface again to remove any disinfectant/residue.
3) Replace the waste collection bin in the Waste Collection station and
close the Waste Collection door.
• 5% bleach solution
1) Dampen a cloth with one of the approved solutions and wipe off any
dust or dirt from the rubber seal on the fill door and its contact surface.
Note: To disinfect a contaminated surface, use a 10% bleach solution and allow it
to remain in contact with the contaminated surface for five minutes.
2) Using plain water, wipe the same surfaces again to remove any
disinfectant residue.
3) Repeat steps one and two to clean the interior surface of the Filler
Station.
• 5% bleach solution
1) Dampen a cloth with one of these approved solutions and wipe the
inside base surface of the instrument, where the cassette is processed.
Note: To disinfect a contaminated surface, use a 10% bleach solution and allow it
to remain in contact with the contaminated surface for five minutes.
2) Dampen a separate cloth with plain water and wipe the surface again to
remove any disinfectant residue.
The system goes through the initialization process. The Status screen
displays a status of OK.
Note: If the instrument was shut down for a long period of time, the status may be
Warming. Wait until the status is OK before resuming test card processing.
This chapter provides information to help you to resolve any problems that
may occur while operating the VITEK® 2 Compact instrument. The first
section, Error Handling System, explains how the instrument reacts to an
error, and how you, the user, should respond. The second section, Contents
of Intervention Messages, defines the types of Intervention messages. Other
sections in this chapter include instrument diagnostics, version and
subsystem error status information, as well as instruction on how to discover
when the instrument was last maintained.
For a list of possible error messages that could occur on the VITEK® 2
Compact instrument, see Appendix C — Instrument Error Code User
Response Table.
Chapter Contents
Troubleshooting Chapter 6:
• Look up the type of intervention screen.
Troubleshooting Chapter 6: • Follow User Response procedure
• Look up error code in Error Code User Note: The dashed arrow indicates a possible
Response Table path.
• Follow User Response procedure
• Error Message Queue — For errors that do not need a user’s immediate
response or that provide details to interventions. This is indicated by a
blinking/audible alert and the moving (!) on the Status screen.
The first element of the Error Handling System is the VITEK® 2 Compact
instrument. The instrument must first detect the error. In many cases, the
instrument attempts to correct the problem by retrying an operation. If that
fails, the instrument selects the appropriate error message, activates the
error alarms, and places the message in the error message queue.
The second element of the Error Handling System is you, the VITEK® 2
Compact user. You must:
• respond to the alarm by accessing the error message queue on the
instrument interface.
• locate the error code from the messages, refer to Appendix C, and follow
the information in the User Response column.
• Visual Alarm. This alarm uses the screen on the interface display. When
the visual alarm is activated, the screen flashes to indicate the presence of
an error condition. An instrument configuration option allows you to select
the visual alarm.
There are two Error Message Queue screens, the first is in a list form and the
second is in detail form. You must review the detailed message to clear the
New Error/Warning indicator.
The queue may contain as many as 250 messages, beginning with the most
recent. Number 001 (Figure 6-2) is the most recent. When a new message is
generated, it assumes number 001 and the other messages move down the
list.
1) To review a message, press the Message Key (!) on the user interface.
• An asterisk (*) to the far left of a message signifies that it has never been
reviewed.
2) Use the Arrow Keys to move the pointer to the desired message. The
Up and Down Arrow keys move the pointer one message at a time. The
Left Arrow key scrolls to the previous page of messages. The Right
Arrow key scrolls to the next page of messages.
3) Press the Message Key (!) again to display the detailed message.
A row of numbers is listed just above a dash line at the bottom of the screen.
The numbers pertain to the error:
Example: 20:13.00.152
• 20 is the primary code
• 152 is the detailed part of the code
You can locate the detailed code number in column one of the VITEK® 2
Compact Instrument Error Code User Response Table in Appendix C.
Review the Error Message queue for any error message the VITEK® 2
Compact instrument has generated. Resolve the problem as indicated in
Appendix C.
Intervention Screen
Note: Some Intervention screens need a timeout counter. This countdown timer
displays on the upper right corner of the Intervention message and indicates
the total number of minutes left for the user to intervene.
Select either:
• Cancel Fill or
• Continue
Select either:
• Cancel Fill or
• Continue
2) Select OK.
2) Select OK.
4) Review any recent errors in the Error Message Queue and refer to
Appendix C for further information.
Note: The OK function button will not appear until the user enters a digit.
2) Select OK.
Note: The OK function button does not appear until the user enters a digit.
When timed out, if the user has not resolved all of the interventions, the
Intervention screen disappears and the cassette continues to process if the
load door is closed. The instrument terminates cards with unresolved bar
code errors, loads the rest of the cards into the carousel, and logs a message
into the Error Message Queue.
If the load door is opened, all cards are terminated and no card is loaded.
2) Select either:
• Clear or
• Accept
Note: The Accept function key does not appear until the user enters a digit.
After timeout, if the user has not entered a cassette ID, the cassette is left in
the loader, the door is closed, and the card bar codes are readable, then the
instrument loads the cards into the carousel, sends a Cassette ID to the
workstation computer, and logs a message in the Error Message Queue.
1) Enter the last two digits of the bar code using the numeric keypad on
the instrument user interface screen:
2 2 2 2 8 8 8 8 3 3 3 3 7 7 7 7 __ __ (example)
2) Select either:
• Skip or
• Accept
Note: If the Skip function is selected, the card(s) specified in the Intervention
screen will not load and is terminated. The instrument returns these cards to
the Cassette Load/Unload station for discard.
The Accept function key appears only after you enter the last two digits
correctly. Use the Left Arrow key to move back, and the Right Arrow key to
move to the next digit, if that digit is already entered.
1) Using the numeric keypad on the instrument user interface screen, enter
the bar code number: _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _
2) Select either:
• Skip or
• Accept
Note: If the Skip function is selected, the card(s) specified in the Intervention
screen will not load and is terminated. They return to the Cassette Load/
Unload station and should be discarded.
The Accept function key appears only after you enter all digits correctly. Use
the Left Arrow key to move back, and the Right Arrow key to move to the
next digit if that digit is already entered.
VC: 1 2 3 4 5 6 7 8 9 0 1 2 3 4 5 6 (example)
1) Remove the cassette from the Cassette Load/Unload Station and locate
the card(s) in the position that was previously entered on the
workstation/host.
2) Reinstall the cassette in the Cassette Load/Unload station, and close the
door.
3) Select either:
• Skip or
• Fixed
Note: If the Skip function is selected, the card(s) specified in the Intervention
screen will not load and is terminated. The instrument returns these cards to
the Cassette Load/Unload station for discard.
Note: [Y] represents the number of cards and [X] represents the card slot number.
4) Select Continue.
Timed Out
1) Remove cassette and close the Cassette Load/Unload door.
3) Select Continue.
1) Select Yes when the Unlock user access door screen appears.
3) Determine the location of the jam (to determine this, review the Error
Message Queue).
WARNING
Unexpected mechanical movement can occur when the jam is
cleared.
4) Resolve any jam conditions and close the User Access Doors.
Instrument Diagnostics
Some of the error recovery procedures in this chapter direct you to perform a
diagnostic test on one of the stations in the VITEK® 2 Compact instrument.
This section tells you how to access and use those tests.
Diagnostic Tests
Following are the tests found on the Diagnostics menu, and their function:
Filler Test
There are times when you may need to run a Filler Test (see Appendix C).
4) At the completion of a successful fill cycle (the Filler’s blue LED blinks),
cancel the cassette using the menu path:
Note: The cancel cassette function will only be active for ten minutes after which
an error will occur. When this error occurs, refer to Appendix C.
The screen displays the Incubator temperature and the temperature inside
the instrument cabinet (Figure 6-9).
This function allows you to view the current instrument firmware version for
your instrument. Customer Support may ask you to supply this information if
you need assistance with any of the recovery procedures.
This function is used to view the last time a field service engineer performed
preventive maintenance. The format is the same as that configured for Date
Format.
This procedure describes how to clean and verify the optics while test cards
are still processing. If the instrument is shut down, you may also clean the
optics. See Cleaning the Optics (Power Off) on page 5-16.
Note: If the cassette is processing in the Filler Station or in the Cassette Load/
Unload Station, the user is not able to unlock the door.
4) When the Front User Access Door is unlocked, both User Access Doors
can be opened to clean the optics.
Note: You have four minutes from the time that you press Yes to complete the
cleaning procedure. A warning message appears if the process exceeds four
minutes.
View the Subsystem Error Status screen when the instrument status is in an
error condition. This screen provides additional details about the error.
Access the Subsystem Error Status screen using the following path:
Power Failure
The UPS notifies VITEK® 2 Compact of a power failure. The instrument then:
• initiates a Power Failure error message and displays a Power Fail icon on
the main status screen.
Hardware Specifications
Mass
VITEK® 2 Compact
Environment
Indoor usage
Do not install in direct sunlight.
Instrument can be placed with its back against the wall, providing nothing is
obstructing the instrument’s fan air flow.
Minimum of 11cm (4.3 in.) clearance on the left and right side.
Electrical Characteristics
Maximum input current 4 amps @ 120 VAC or 2.2 amps @ 240 VAC
Nominal input current 2.5 amps @ 120 VAC or 1.25 amps @ 240 VAC
Optical Characteristics
Transmittance Optics
Emission wavelengths: 660 nm, 568 nm, 428 nm LED
WARNING
There is a potential for non-laser optical energy emanation from
the optics which could result in personal injury or damage to
the instrument.
General Characteristics
Cassette
Capacity, cards: 10 cards per cassette
Vacuum (Filler)
Minimum level: 0.89 PSIA ± 0.06 PSIA
Sealer
Mechanical: stub length 1.25 ± 0.25 mm
Incubator
Temperature: 35.5 °C ± 1 °C average
Capacity: 15, 30, or 60 cards per Incubator (depending on configuration)
The maintenance log provided on the following pages can be used to record
and document the maintenance items listed.
Day of Month: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16
Maintenance Log
Clean Carousel *
Clean Cassettes*
Clean Optics *
Check Instrument QC
Status Report for the
Carousel Temperature **
Optics Systems**
* = Monthly ** = Daily
Appendix B
24410
VITEK® 2 Compact Instrument User Manual
VITEK® 2 Compact Maintenance Log Month____________ Year____________
24410
Appendix B
Day of Month: 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31
Clean Carousel *
Clean Cassettes*
Clean Optics *
Check Instrument QC
Status Report for the
Carousel Temperature **
Optics Systems**
* = Monthly ** = Daily
B-3
Maintenance Log
Maintenance Log Appendix B
1) Locate the detail code from the Error Message Queue screen described
in Chapter 6.
2) Find the Detail Code from the first column of the table. Detail codes are
listed numerically.
4) Read and follow the directions found in the User Response column of
the table and address accordingly.
Table C-1: VITEK® 2 Compact Instrument Error Code User Response Table
1 NA <unused> NA
12 12 Software Instrument Failure This warning indicates that an internal software resource
Warning has fallen below the expected minimum level. The
instrument is still functioning normally.
Report to bioMérieux.
13 1 Software Failure Bar Code Reader The instrument is in a fault condition. Call bioMérieux.
failure A field service visit is likely required.
14 3 Vacuum/Loader Bar Code Reader The instrument is in a fault condition. Call bioMérieux.
Failure failure A field service visit is likely required.
15 8 Autoloader Jam Autoloader motor This may be the result of a jam due to foreign material in
failed to home the mechanism, or it may indicate a mechanical or
electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors and/or load door.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
16 7 Transport Jam Transport motor This may be the result of a jam due to foreign material in
failed to home the mechanism, or it may indicate a mechanical or
during electrical failure.
initialization 1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors and/or load door.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
17 7 Transport Jam Transport motor This may be the result of a jam due to foreign material in
failed to home the mechanism, or it may indicate a mechanical or
during loading electrical failure.
(after cassette 1) Respond to the Intervention screen for the jam
inspection) condition.
2) Open user access doors and/or load door.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
18 9 Sealer Jam Sealer motor This may be the result of a jam due to foreign material in
failed to home the mechanism, or it may indicate a mechanical or
electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors and/or load door.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
23 13 Load Door Load Door open Close door and cycle power.
Open while attempting
initialization
24 13 Load Door Load Door open Close door and cycle power.
Open while attempting
to initiate a
cassette load
25 3 Vacuum/Loader Load Door will not Ensure that the Load Door is fully closed. Check the
Failure lock latching mechanism for foreign materials.
27 NA <unused> NA
28 7 Transport Jam Cassette is not This may be the result of a jam due to foreign material in
hooked on the mechanism, or it may indicate a mechanical or
transport block electrical failure.
pins during 1) Respond to the Intervention screen for the jam
initialization condition.
2) Open user access doors and/or load door.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
29 7 Transport Jam Transport motor This may be the result of a jam due to foreign material in
stalled while the mechanism, or it may indicate a mechanical or
counting cards electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors and/or load door.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
30 NA <unused> NA
31 7 Transport Jam Transport motor This may be the result of a jam due to foreign material in
stalled while the mechanism, or it may indicate a mechanical or
reading card bar electrical failure.
code 1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors and/or load door .
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
32 7 Transport Jam Transport motor This may be the result of a jam due to foreign material in
stalled while the mechanism, or it may indicate a mechanical or
moving cassette electrical failure.
toward load door 1) Respond to the Intervention screen for the jam
during bar code condition.
retry 2) Open user access doors and/or load door.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
33 7 Transport Jam Transport motor This may be the result of a jam due to foreign material in
stalled while the mechanism, or it may indicate a mechanical or
moving cassette electrical failure.
toward load door 1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors and/or load door.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
34 7 Transport Jam Transport motor This may be the result of a jam due to foreign material in
stalled while the mechanism, or it may indicate a mechanical or
sealing electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors and/or load door.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
35 7 Transport Jam Transport motor This may be the result of a jam due to foreign material in
stalled while the mechanism, or it may indicate a mechanical or
loading cards into electrical failure.
carousel 1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors and/or load door.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
36 7 Transport Jam Transport motor This may be the result of a jam due to foreign material in
stalled while the mechanism, or it may indicate a mechanical or
unloading cassette electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors and/or load door.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
37 8 Autoloader Jam Autoloader motor This may be the result of a jam due to foreign material in
stalled while the mechanism, or it may indicate a mechanical or
loading cards into electrical failure.
carousel 1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors and/or load door.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
41 NA <unused> NA
57 15 Carousel Cover Carousel cover is Ensure that the carousel cover is properly installed.
Missing missing during
pre-initialization
check
58 15 Carousel Cover Carousel cover Ensure that the carousel cover is properly installed.
Missing missing during
carousel
initialization
59 15 Carousel Cover Carousel cover This may be the result of a jam due to foreign material in
Missing detected missing the mechanism, or it may indicate a mechanical or
during move electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
60 14 User Access User access door Close door and cycle power.
Door Open is open during
initialization
61 3 Vacuum/Loader User access door Ensure that the user access door is fully closed. Check the
Failure will not lock latching mechanism for foreign materials.
63 18 Carousel Quad missing Referring to the carousel cleaning section of this manual,
Section Missing during ensure that all quads are properly installed.
initialization
64 6 Carousel Jam Carousel motor This may be the result of a jam due to foreign material in
failed to home the mechanism, or it may indicate a mechanical or
during electrical failure.
initialization 1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
66 5 Reader Jam Ejector motor This may be the result of a jam due to foreign material in
failed to home the mechanism, or it may indicate a mechanical or
during electrical failure.
initialization 1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
67 5 Reader Jam Cam motor failed This may be the result of a jam due to foreign material in
to home during the mechanism, or it may indicate a mechanical or
initialization electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
68 1 Software Failure Instrument failure Call bioMérieux. A power cycle may be required.
69 1 Software Failure Instrument failure Call bioMérieux. A power cycle may be required.
70 1 Software Failure Instrument failure Call bioMérieux. A power cycle may be required.
71 1 Software Failure Instrument failure Call bioMérieux. A power cycle may be required.
72 17 Card(s) All cards unloaded The instrument is in a fault condition. Call bioMérieux.
Terminated due to incubator A field service visit is likely required.
temperature fault,
carousel position
lost or unload via
DML
74 6 Carousel Jam Carousel motor This may be the result of a jam due to foreign material in
stalled the mechanism, or it may indicate a mechanical or
electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
76 37 The card in slot Wellmap does not This card is rejected (and terminated) due to the wellmap
(X) of cassette (X) exist for a card not being present.
was rejected during cassette
because this inspection Enter the needed wellmap before attempting to process
instrument did any further cards of this type.
not have an
appropriate
wellmap
78 17 Card(s) Could not find the A card edge or hole could not be found. The card in this
Terminated first edge of the carousel slot is terminated. When instrument processing is
card (terminated idle, perform a carousel cleaning to gain access to the card
slot) and make the slot available.
79 5 Reader Jam Could not find the This may be the result of a jam due to foreign material in
first edge of the the mechanism, or it may indicate a mechanical or
card (JAMMED) electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
80 17 Card(s) Each optical A card edge or hole could not be found. The card in this
Terminated position mark was carousel slot was terminated. When instrument processing
not detected in is idle, perform a carousel cleaning to gain access to the
the card while card and make the slot available.
moving out
(terminated slot)
81 5 Reader Jam Each optical This may be the result of a jam due to foreign material in
position mark was the mechanism, or it may indicate a mechanical or
not detected in electrical failure.
the card while 1) Respond to the Intervention screen for the jam
moving out condition.
(JAMMED) 2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
84 19 Waste Bucket Could not unload Replace the waste bin and close waste door.
Full or Waste Door card, waste bin is
Open not present
85 19 Waste Bucket Could not unload Ensure that the waste bin is empty, present, and that the
Full or Waste Door card, waste chute waste door is closed. Check to be sure there are no cards
Open is clogged remaining in the waste chute.
86 19 Waste Bucket Failed to eject card Ensure that the waste bin is empty, present, and that the
Full or Waste Door into waste bin waste door is closed. Check to be sure there are no cards
Open (card was still in remaining in the waste chute.
read head)
87 5 Reader Jam Failed to place the This may be the result of a jam due to foreign material in
card back into the mechanism, or it may indicate a mechanical or
carousel while electrical failure.
verifying the head 1) Respond to the Intervention screen for the jam
was clear condition.
(JAMMED) 2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
88 5 Reader Jam Could not find the This may be the result of a jam due to foreign material in
first edge of the the mechanism, or it may indicate a mechanical or
card while reading electrical failure.
(JAMMED) 1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
89 17 Card(s) Could not find the A card edge or hole could not be found. The card in this
Terminated first edge of the carousel slot was terminated. When instrument processing
card while reading is idle, perform a carousel cleaning to gain access to the
(terminated slot) card and make the slot available.
90 5 Reader Jam Each optical This may be the result of a jam due to foreign material in
position mark the mechanism, or it may indicate a mechanical or
(Air) was not electrical failure.
detected while 1) Respond to the Intervention screen for the jam
reading (JAMMED) condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
91 17 Card(s) Each optical A card edge or hole could not be found. The card in this
Terminated position mark carousel slot was terminated. When instrument processing
(Air) was not is idle, perform a carousel cleaning to gain access to the
detected while card and make the slot available.
reading
(terminated slot)
92 5 Reader Jam Each optical This may be the result of a jam due to foreign material in
position mark the mechanism, or it may indicate a mechanical or
(Plastic) was not electrical failure.
detected while 1) Respond to the Intervention screen for the jam
reading (JAMMED) condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
93 17 Card(s) Each optical A card edge or hole could not be found. The card in this
Terminated position mark carousel slot is terminated. When instrument processing is
(Plastic) was not idle, perform a carousel cleaning to gain access to the card
detected while and make the slot available.
reading
(terminated slot)
94 5 Reader Jam The last edge of 1) This may be the result of a jam due to foreign material
the card was not in the mechanism, or it may indicate a mechanical or
detected while electrical failure. Respond to the Intervention screen for
reading (JAMMED) the jam condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
95 17 Card(s) The last edge of A card edge or hole could not be found. The card in this
Terminated the card was not carousel slot was terminated. When instrument processing
detected while is idle, perform a carousel cleaning to gain access to the
reading card and make the slot available.
(terminated slot)
96 5 Reader Jam An additional row This may be the result of a jam due to foreign material in
was detected the mechanism, or it may indicate a mechanical or
while reading electrical failure.
(JAMMED) 1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
97 17 Card(s) An additional row A card edge or hole could not be found. The card in this
Terminated was detected carousel slot was terminated. When instrument processing
while reading is idle, perform a carousel cleaning to gain access to the
(terminated slot) card and make the slot available.
98 5 Reader Jam Cam failure while This may be the result of a jam due to foreign material in
reading (JAMMED) the mechanism, or it may indicate a mechanical or
electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
99 5 Reader Jam Cam failure This may be the result of a jam due to foreign material in
(JAMMED) the mechanism, or it may indicate a mechanical or
electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
100 5 Reader Jam Cam failure This may be the result of a jam due to foreign material in
(JAMMED) the mechanism, or it may indicate a mechanical or
electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
101 5 Reader Jam Carousel jam after This may be the result of a jam due to foreign material in
a Cam failure the mechanism, or it may indicate a mechanical or
(JAMMED) electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
102 5 Reader Jam Cam failure This may be the result of a jam due to foreign material in
(JAMMED) the mechanism, or it may indicate a mechanical or
electrical failure.
1) Respond to the Intervention screen for the jam
condition.
2) Open user access doors.
3) Examine the affected component for dirt or obstruction
(normal jam-clearing actions).
4) If this is related to a transport jam, reposition the
cassette on the transport block before closing door.
5) If the failure reoccurs, call bioMérieux.
103 4 Carousel/ Head Control The instrument is in a fault condition. Call bioMérieux.
Reader Failure Board failure A field service visit is likely required.
104 43 Optics Transmittance Ensure that the TX optics modules are closed and perform
problem (may Optics module TX optics cleaning.
need cleaning) TX1 failed
calibration
105 43 Optics Transmittance Ensure that the TX optics modules are closed and perform
problem (may Optics module TX optics cleaning.
need cleaning) TX2 failed
calibration
106 43 Optics Transmittance Ensure that the TX optics modules are closed and perform
problem (may Optics module TX optics cleaning.
need cleaning) TX3 failed
calibration
107 43 Optics Transmittance Ensure that the TX optics modules are closed and perform
problem (may Optics module TX optics cleaning.
need cleaning) TX1 position
sensor not
functional
108 43 Optics Transmittance Ensure that the TX optics modules are closed and perform
problem (may Optics module TX optics cleaning.
need cleaning) TX2 position
sensor not
functional
109 43 Optics Transmittance Ensure that the TX optics modules are closed and perform
problem (may Optics module TX optics cleaning.
need cleaning) TX3 position
sensor not
functional
110 21 Optics Almost Transmittance The instrument is still functioning normally, however
Out of Calibration Optics module perform optics cleaning.
TX1 nearing
calibration limits
111 21 Optics Almost Transmittance The instrument is still functioning normally, however
Out of Calibration Optics module perform optics cleaning.
TX2 nearing
calibration limits
112 21 Optics Almost Transmittance The instrument is still functioning normally, however
Out of Calibration Optics module perform optics cleaning.
TX3 nearing
calibration limits
113 43 Optics Transmittance Ensure that the TX optics modules are closed and perform
problem (may Optics module TX optics cleaning.
need cleaning) TX1 is not
available to
process this card
114 43 Optics Transmittance Ensure that the TX optics modules are closed and perform
problem (may Optics module TX optics cleaning.
need cleaning) TX2 is not
available to
process this card
115 43 Optics Transmittance Ensure that the TX optics modules are closed and perform
problem (may Optics module TX optics cleaning.
need cleaning) TX3 is not
available to
process this card
116 43 Optics Transmittance Ensure that the TX optics modules are closed and perform
problem (may Optics module TX optics cleaning.
need cleaning) TX1 reference
readings out of
range
117 43 Optics Transmittance Ensure that the TX optics modules are closed and perform
problem (may Optics module TX optics cleaning.
need cleaning) TX2 reference
readings out of
range
118 43 Optics Transmittance Ensure that the TX optics modules are closed and perform
problem (may Optics module TX optics cleaning.
need cleaning) TX3 reference
readings out of
range
122 11 Internal Data Carousel Map The instrument is in a fault condition. Call bioMérieux.
Error memory failure A field service visit is likely required.
123 11 Internal Data Carousel Map The instrument is in a fault condition. Call bioMérieux.
Error memory failure A field service visit is likely required.
124 11 Internal Data Carousel Map The instrument is in a fault condition. Call bioMérieux.
Error memory failure A field service visit is likely required.
125 11 Internal Data Cassette memory The instrument is in a fault condition. Call bioMérieux.
Error failure A field service visit is likely required.
126 12 Software Memory failure Some card reading data may be lost due to a power
Warning failure, software crash, or turning off the instrument
without first performing the shutdown process.
127 11 Internal Data Memory failure The instrument is in a fault condition. Call bioMérieux.
Error A field service visit is likely required.
128 11 Internal Data Memory failure The instrument is in a fault condition. Call bioMérieux.
Error A field service visit is likely required.
129 12 Software Memory failure Some card reading data may be lost due to loss of
Warning communications with the host computer.
130 11 Internal Data Memory failure The instrument is in a fault condition. Call bioMérieux.
Error A field service visit is likely required.
131 11 Internal Data Memory failure The instrument is in a fault condition. Call bioMérieux.
Error A field service visit is likely required.
132 11 Internal Data Memory failure The instrument is in a fault condition. Call bioMérieux.
Error A field service visit is likely required.
133 11 Internal Data Memory failure The instrument is in a fault condition. Call bioMérieux.
Error A field service visit is likely required.
134 11 Internal Data Memory failure The instrument is in a fault condition. Call bioMérieux.
Error A field service visit is likely required.
135 11 Internal Data Memory failure The instrument is in a fault condition. Call bioMérieux.
Error A field service visit is likely required.
136 11 Internal Data Memory failure The instrument is in a fault condition. Call bioMérieux.
Error A field service visit is likely required.
137 11 Internal Data Memory failure The instrument is in a fault condition. Call bioMérieux.
Error A field service visit is likely required.
138 11 Internal Data Memory failure The instrument is in a fault condition. Call bioMérieux.
Error A field service visit is likely required.
143 11 Internal Data Memory failure The instrument is in a fault condition. Call bioMérieux.
Error A field service visit is likely required.
146 22 Hardware SPN board failure The instrument is in a fault condition. Call bioMérieux.
Failure A field service visit is likely required.
147 NA <unused> NA
148 NA <unused> NA
149 NA <unused> NA
150 NA <unused> NA
151 NA <unused> NA
152 20 Doors opened Emergency Stop – A door was opened while locked. As this could present a
while processing door open while hazard to the user, all instrument operations are halted.
– Emergency Stop locks engaged
occurred Ensure doors are closed and then cycle power to the
instrument.
153 22 Hardware RTC and CPU Xtal The instrument is in a fault condition. Call bioMérieux.
Failure cross-check failure A field service visit is likely required.
– frequency
mismatch
155 22 Hardware Power Supply Ensure that the instrument’s ambient temperature
Failure Temperature High specifications are not exceeded.
156 24 UPS power UPS indicates a A power failure has occurred and the instrument is
failure or battery power failure has operating on the UPS battery.
bad occurred
157 24 UPS power UPS Battery has The battery in the UPS may be defective.
failure or battery failed
bad Call bioMérieux.
158 22 Hardware Cabinet intake fan The instrument is in a fault condition. Call bioMérieux.
Failure is rotating too A field service visit is likely required.
slowly.
159 22 Hardware Cabinet exhaust The instrument is in a fault condition. Call bioMérieux.
Failure fan is rotating too A field service visit is likely required.
slowly.
160 23 Incubator Incubator heater The instrument is in a fault condition. Call bioMérieux.
failure fan is rotating too A field service visit is likely required.
slowly.
163 25 Filler failure Fill cycle failure The instrument is in a fault condition. Call bioMérieux. A
field service visit is likely required.
164 25 Filler failure Fill cycle failure The instrument is in a fault condition. Call bioMérieux. A
field service visit is likely required.
165 25 Filler failure Insufficient Enter cassette ID as prompted and discard cards.
vacuum level
achieved during Ensure that the door seal on the vacuum filler is clean,
fill cycle then perform filler test.
166 25 Filler failure Incorrect up slope Enter cassette ID as prompted and discard cards.
during fill cycle
Ensure that the door seal on the vacuum filler is clean,
then perform filler test.
167 25 Filler failure Incorrect down Enter cassette ID as prompted and discard cards.
slope during fill
cycle Ensure that the door seal on the vacuum filler is clean,
then perform filler test.
168 25 Filler failure Fill cycle failure Enter cassette ID as prompted and discard cards.
169 25 Filler failure Fill cycle failure The instrument is in a fault condition. Call bioMérieux.
A field service visit is likely required.
170 26 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) removed from the processing.
will not be loaded cassette during a
because it was power failure and
not detected after replaced with
a power failure another card.
171 26 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) removed from the processing.
will not be loaded cassette during a
because it was power failure.
not detected after
a power failure
172 27 The card in slot The card was no Discard the identified card(s).They were not accepted for
(X) of cassette (X) longer readable processing.
will not be loaded after a power
because it could failure.
not be scanned
after a power
failure
173 28 The card in slot The card was not Discard the identified card(s). They were not accepted for
(X) of cassette (X) loaded in the time processing.
will not be loaded allowed. (Power
because it Failure)
exceeded the
loading timeout
174 28 The card in slot The card was not Discard the identified card(s). They were not accepted for
(X) of cassette (X) loaded in the time processing.
will not be loaded allowed. (Power
because it Failure)
exceeded the
loading timeout
175 29 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) being sealed processing.
will not be loaded when a
because it mechanical error
encountered a occurred. (Power
mechanical error Failure)
while sealing
176 NA <unused> NA
177 29 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) being sealed processing.
will not be loaded when a transport
because it mechanical error
encountered a occurred. (Alarm)
mechanical error
while sealing
178 29 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) being sealed processing.
will not be loaded when a transport
because it mechanical error
encountered a occurred. (jam)
mechanical error
while sealing
179 30 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) rejected because processing.
was rejected the card is expired.
because it has
expired
180 31 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) rejected because processing.
was rejected of insufficient
because of carousel capacity.
insufficient
carousel capacity
181 32 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) rejected because it processing.
was rejected was introduced in
because it was place of another
introduced after card during a
the cards in the power failure.
cassette were
sealed
182 32 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) rejected because it processing.
was rejected was introduced
because it was where no previous
introduced after card was during a
the cards in the power failure.
cassette were
sealed
183 33 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) rejected because processing.
was rejected the instrument
because this does not have the
instrument is not required optics.
configured with
the required
optics
184 34 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) defined and was processing.
was rejected not detected
because a virtual during processing.
card was defined
for that slot and
not detected
185 35 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) rejected because it processing.
was rejected mismatched the
because the definition.
scanned card did
not match the
virtual card
defined for that
slot
186 36 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) rejected because it processing.
was rejected mismatched the
because the definition during a
scanned card did timeout.
not match the
virtual card when
the cassette timed
out
187 37 The card in slot The card was Discard the card(s).
(X) of cassette (X) rejected because
was rejected the instrument did The “Maintain AST definitions” data entry for this card type
because this not have a proper should be performed before attempting to process
instrument did wellmap. additional cards of this type.
not have an
appropriate
wellmap
188 40 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) rejected because processing.
was not loaded the cassette load
due to a biological timer timed out.
timeout
189 40 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) rejected because processing.
was not loaded the cassette load
due to a biological timer timed out
timeout over a power
failure.
190 41 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) rejected because processing.
was not loaded the intervention
because it timed timer timed out
out and was and the Bar Code
unreadable was unreadable.
191 42 The card in slot The card was Discard the identified card(s). They were not accepted for
(X) of cassette (X) rejected (user processing.
was rejected skipped).
192 38 Cassette (X) The cassette Discard the card(s) in the specified cassette. They were
was aborted by transfer was not accepted for processing.
the user aborted by the
user.
193 39 Cassette (X) A filling failure Discard the card(s) in the specified cassette. They were
was terminated occurred (cassette not accepted for processing.
due to a fill failure cancelled)
194- 44 Component NA Instrument errors of this type should not occur in normal
218 Stats processing mode. (Factory only.)
227 46 Cassette (X) The Cassette was Discard the card(s) in the specified cassette. They were
was not not transferred in not accepted for processing.
transferred to the the allotted time.
loader within the (10 Minutes)
appropriate time.
228 47 The scanned The scanned This error indicates that after a power failure or clearing of
cassette ID did cassette ID did not a jam, the cassette ID that was scanned does not match
not match the match the the original ID that was scanned or user-entered.
stored cassette ID scanned ID
while verifying an If the bar code of the cards match the originally scanned
accepted cassette. bar codes, this error is informational only. If they did not
match, other errors relating to those cards rejections are
logged. This error code provides information only.
229 48 Cassette (X) A cassette was Discard the card(s) in the specified cassette. They were
was filling when filling when a not accepted for processing.
power failed and power failure
has been occurred.
discarded.
230 1 Software Failure Instrument failure Call bioMérieux. A power cycle may be required.
231 28 The card in slot The card was not Discard the card(s) in the specified cassette. They were
(X) of cassette (X) loaded in the time not accepted for processing.
will not be loaded allowed. (power
because it failure).
exceeded the
loading timeout
232 1 Software Failure Reboots halted The instrument is in a fault condition. Call bioMérieux.
due to repeating A field service visit is likely required.
error
233 22 Hardware SPN board failure The instrument is in a fault condition. Call bioMérieux.
Failure A field service visit is likely required.
234 22 Hardware SPN board failure The instrument is in a fault condition. Call bioMérieux.
Failure A field service visit is likely required.
235 22 Hardware Emergency Stop – The instrument is in a fault condition. Call bioMérieux.
Failure Front Panel SPN A field service visit is likely required.
board failure
236 - 44 Component NA Instrument errors of this type should not occur in normal
241 Stats processing mode. (Factory only.)
242 49 A fill was A vacuum was not Ensure that the door seal on the vacuum filler is clean and
stopped because achieved during a then re-try the filling operation.
no vacuum was fill.
achieved (Clean
the Seal).
249 4 Carousel/ SPN board failure The instrument is in a fault condition. Call bioMérieux.
Reader Failure A field service visit is likely required.
250 3 Vacuum/Loader SPN board failure The instrument is in a fault condition. Call bioMérieux.
Failure A field service visit is likely required.
251 3 Vacuum/Loader SPN board failure The instrument is in a fault condition. Call bioMérieux.
Failure A field service visit is likely required.
252 22 Hardware SPN board failure The instrument is in a fault condition. Call bioMérieux.
Failure A field service visit is likely required.
253 40 The card in slot The card was The cards were not loaded, probably due to a power
(X) of cassette (X) rejected because failure or jam recovery. Discard the card(s) in the specified
was not loaded the first read timer cassette. They were not accepted for processing.
due to a biological timed out.
timeout
254 40 The card in slot The card was The cards were not loaded, probably due to a power
(X) of cassette (X) rejected because failure or jam recovery. Discard the card(s) in the specified
was not loaded the first read timer cassette. They were not accepted for processing.
due to a biological timed out.
timeout
255 41 The card in slot The card was Discard the card(s) specified. They were not accepted for
(X) of cassette (X) rejected because processing.
was not loaded the intervention
because it timed timer timed out
out and was and the bar code
unreadable was unreadable.
256 1 Software Failure Instrument failure Call bioMérieux. A power cycle may be required.
258 51 The card in slot The Cassette was Discard the card(s) specified. They were not accepted for
(X) of cassette (X) removed over a processing.
was terminated power failure
because the while it was in
cassette was not process.
present after a
power failure.
259 1 Software Failure Instrument failure Call bioMérieux. A power cycle may be required.
260- 45 BurnIn NA Instrument errors of this type should not occur in normal
261 processing mode. (Factory only.)
262 1 Software Failure Instrument failure Call bioMérieux. A power cycle may be required.
263 40 The card in slot The card was Discard the card(s) specified. They were not accepted for
(X) of cassette (X) rejected because processing.
was not loaded the first read timer
due to a biological timed out (power
timeout failure).
264 40 The card in slot The card was Discard the card(s) specified. They were not accepted for
(X) of cassette (X) rejected because processing.
was not loaded the cassette load
due to a biological timer timed out
timeout (power failure).
265 41 The card in slot The card was Discard the card(s) specified. They were not accepted for
(X) of cassette (X) rejected because processing.
was not loaded the intervention
because it timed timer timed out
out and was and the Bar Code
unreadable was unreadable
(power failure).
266 42 The card in slot The card was Discard the card(s) specified. They were not accepted for
(X) of cassette (X) rejected because it processing.
was rejected has a duplicate in
the cassette or
carousel.
267 42 The card in slot The card was Discard the card(s) specified. They were not accepted for
(X) of cassette (X) rejected because processing.
was rejected the cassette is out
of alignment.
268 3 Vacuum/Loader Sealer failure The instrument is in a fault condition. Call bioMérieux.
Failure A field service visit is likely required.
269 3 Vacuum/Loader Sealer failure The instrument is in a fault condition. Call bioMérieux.
Failure A field service visit is likely required.
270- 44 Component NA Instrument errors of this type should not occur in normal
271 Stats processing mode. (Factory only.)
272 10 Host No response from Workstation may be turned off or may not be connected.
Communication the Workstation Check the power on the PC and be sure the data cable is
Failure PC for 1 hour. secure.
Bar Code Reader This station reads the bar code label on each cassette and test
(Instrument) card after the test cards are loaded into the Cassette Load/
Unload Station. It then transfers all of the test card bar code
data to the VITEK® 2 Compact Workstation computer.
Filler Station The Filler Station inoculates all of the cards in a cassette with
the suspension contained in their corresponding test tubes. It
uses a vacuum chamber and air pump.
Sealer Station This station seals each test card by cutting and sealing its
associated inoculum transfer tube using a hot wire.
Test Card A plastic card with 64 growth wells for biological testing in
VITEK® 2 systems. Each well contains an air-dried suspension
of a biochemical or antibiotic.
User Access Doors VITEK® 2 Compact has two doors to enable the operator to
access the internal systems and stations to perform
maintenance and cleaning procedures: Top User Access Door
and Front User Access Door.
User interface (UI) The portion of the system in which the user and the system’s
software interact. The system has two user interfaces:
• Workstation computer, consisting of a monitor, keyboard,
and mouse.
Waste Collection Station This station includes a waste collection bin which holds up to
60 test cards. Ejected test cards are collected in the bin for
removal from the instrument and disposal.
Intervention Log
alert category 3-10 maintenance B-1
card processing 6-7
during filing 6-7 M
screen layouts 6-7
timeout status 6-7
Maintenance
date 6-16
Introduction instrument 5-1
configuration options 3-1 log B-1
manual 1-1
Manual
audience 1-3
J finding topics 1-4
Jam introduction 1-1
card processing 6-12 organization 1-3
purpose 1-2
standard symbols 1-6
K usage 1-1
Key Menu system 2-20
error/message 2-19 Message
previous screen 2-19
card barcode unreadable 6-10
Keyclick Volume 3-13 card code mismatch 6-11
setting 3-14 card processing jam 6-12
Name Replacing
instrument 3-3 waste collection bin 4-17