PlainRecalls
FDA Devices Moderate Class II Ongoing

VITEK 2 REAGENT AST-GN79 TEST KIT 20 CARDS, CATALOG 413436

Reported: January 11, 2023 Initiated: November 9, 2022 #Z-0836-2023

Product Description

VITEK 2 REAGENT AST-GN79 TEST KIT 20 CARDS, CATALOG 413436

Reason for Recall

As the temperature and time out of range was exceeded, product performances cannot be guaranteed

Details

Recalling Firm
Biomerieux Inc
Units Affected
310 units
Distribution
US Nationwide distribution.
Location
Hazelwood, MO

Frequently Asked Questions

What product was recalled?
VITEK 2 REAGENT AST-GN79 TEST KIT 20 CARDS, CATALOG 413436. Recalled by Biomerieux Inc. Units affected: 310 units.
Why was this product recalled?
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
Which agency issued this recall?
This recall was issued by the FDA Devices on January 11, 2023. Severity: Moderate. Recall number: Z-0836-2023.