FDAApril 20, 2017device

VITEK 2 Gram-Positive identification card (GP), IVD, REF 21342, 20 cards per carton.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).

What to do

FDA enforcement status: Terminated

Brands named

biomerieux

UPCs

242015710302242016410309242016910314242017420319242018510330242019820312242020010314242020410318242020510319242022020304242022920313242023920323

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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