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

Recall Z-0808-2013 — Oxoid Antimicrobial Susceptibility Discs, Cefoxitin 30ug REF CT0119B, packaged with 50 discs per cartridge, 5 cartridges per box. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hants, UK.

U.S. FDA — Device Enforcement · United States · 2012-08-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0808-2013
Date of alert
2012-08-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Remel Inc
Product category
device
Product type
Devices
Reported risk: The firm is recalling the product because the cartridges may contain discs that have an insufficient dose of antibiotic.
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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