PlainRecalls
FDA Devices Moderate Class II Ongoing

VITEK 2 REAGENT BCL TEST KIT VTK2 20 CARDS, CATALOG 21345

Reported: January 11, 2023 Initiated: November 9, 2022 #Z-0790-2023

Product Description

VITEK 2 REAGENT BCL TEST KIT VTK2 20 CARDS, CATALOG 21345

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
1 unit
Distribution
US Nationwide distribution.
Location
Hazelwood, MO

Frequently Asked Questions

What product was recalled?
VITEK 2 REAGENT BCL TEST KIT VTK2 20 CARDS, CATALOG 21345. Recalled by Biomerieux Inc. Units affected: 1 unit.
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-0790-2023.