bioMerieux, Inc. recalls VITEK 2 AST-N351 Test Kit
- Recall date
- December 13, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0847-2019
- FDA classification
- Class II
- Brand / firm
- bioMerieux, Inc.
- Sold / distributed
- UK and Ireland
Why it was recalled
False Positive ESBL Phenotype
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
VITEK 2 AST-N351 Test Kit
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