Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1137-2019 — Biomerieux Vitek 2 Test kit VITEK 2 is an automated system consisting of instruments, software and reagent cards designed for the identification and antimicrobial susceptibility testing of bacteria and yeast.

U.S. FDA — Device Enforcement · United States · 2019-03-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1137-2019
Date of alert
2019-03-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
bioMerieux, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
03573026404550
Reported risk: Unexpected ESBL (Extended Spectrum Beta Lactamase) phenotype had been proposed for some Escherichia coli strains in conjunction with the VITEK 2 AST-N254, AST-N330, AST-N371 (ref.413723,418674, 422024) test kits.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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