Devices

Device Recall Vitek 2 ASTP641 REF 418 590

Model / Serial
lot 741350820, expiration 22JUL16; lot 741340920, expiration 14APR16;
Product Classification
Immunology and Microbiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution to United Kingdom and Turkey. NO U.S. distribution.
Product Description
Vitek 2 AST-P641 REF 418 590 Gram Positive Susceptibility Card, 20 cards per carton, IVD. || Intended for use with the Vitek 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of Staphylococcus spp., Enterococcus spp., and S. agalactiae.
Manufacturer
Biomerieux Inc
1 Event
- Recall of Device Recall Vitek 2 ASTP641 REF 418 590

Manufacturer

Biomerieux Inc

Manufacturer Address
Biomerieux Inc, 595 Anglum Rd, Hazelwood MO 63042-2320
Manufacturer Parent Company (2017)
Compagnie Merieux Alliance
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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