RecallRadar

FDA Device recall Z-0991-2013

VITEK 2 Compact computer system when equipped with the following Hewlett-Packard PC models: (1) dc7100 8-port, Cat. #W0441

On 2013-04-03 the FDA classified a Class II recall of VITEK 2 Compact computer system when equipped with the following Hewlett-Packard PC models: (1) dc7100 8-port, Cat. #W0441 by Biomerieux, citing there is a potential to link an isolate result to the wrong patient and then upload the results to the LIS.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-0991-2013
ClassificationClass II
Statusterminated
Initiated2013-02-18
Published2013-04-03
Last updated2026-09-13 11:53 UTC
CompanyBiomerieux
DistributionUS

Product

VITEK 2 Compact computer system when equipped with the following Hewlett-Packard PC models: (1) dc7100 8-port, Cat. #W0441; (2) dc7100 8-port (refurbished), Cat. #W0441R; (3) dc7700 8-port, Cat. #W0447; (4) dc7700 8-port (refurbished), Cat. #W0447R; (5) dc7800, Cat. #W0449; (6) dc7800 (refurbished), Cat. #W0449R (7) rp5700, Cat. #W0452; (8) rp5700 (refurbished), Cat. #W0452R; (9) rp5800 XPE, Cat. 413642; (10) rp5800WES7, Cat. #413862; (11) d530 6-port, Cat. #W0438; (12) d530 6-port (refurbished), Cat. #W0438R; and (13) d530 4-port, Cat. #W0437. VITEK 2 is an automated system designed for the identification and antimicrobial susceptibility testing of bacteria and yeast.

Reason

There is a potential to link an isolate result to the wrong patient and then upload the results to the LIS.

Identifiers

code_infoManufactured from September, 2004, to present.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0991-2013%22

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