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

Recall Z-2380-2017 — VITEK¿ 2 Gram Negative Susceptibility card (AST-GN49), REF 412091, 20 cards per carton.

U.S. FDA — Device Enforcement · United States · 2017-04-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2380-2017
Date of alert
2017-04-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Biomerieux Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
4690028203
Reported risk: The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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