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

Recall Z-2081-2013 — Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin), Cat. #CT0036B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England Product is used in the semi-quantitative agar diffusion test method for in-vitro su

U.S. FDA — Device Enforcement · United States · 2013-03-25 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2081-2013
Date of alert: 2013-03-25
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: Remel Inc
Product category: device
Product type: Devices

Reported risk: Use of affected lots may give false indication of susceptibility to Nitrofurantoin.

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.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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