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bioMerieux, Inc. recalls VITEK 2 AST-N351 Test Kit
Recalled February 27, 2019 · FDA recall Z-0847-2019 · bioMerieux
Hazard
False Positive ESBL Phenotype · FDA Class II
Units
30,292 cartons (20 cards per carton)
Sold at
UK and Ireland
Description
False Positive ESBL Phenotype
Product
VITEK 2 AST-N351 Test Kit
Manufacturer(s)
bioMerieux, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →