Biomerieux Inc recalls VITEK 2 Bacillus identification card (BCL), IVD, REF 21345,
See all recalls from Biomerieux Inc →Recalled Product
VITEK 2 Bacillus identification card (BCL), IVD, REF 21345, 20 cards per carton.
Hazard / Issue
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: 2390150203 25/Apr/18
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for VITEK 2 Bacillus identification →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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