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

Recall Z-1251-2016 — IMCO brand Conforming Stretch Gauze Bandages, 4 x 4.1 Yds/10 cm x 3,7 cm, Reorder No. 704-IMC, Bar code 6 86864 04351 5, 96 per case (8 boxes x 12 sterile bandages), Single Use To cover and protect the primary dressing that is in contact with wounds from further injuries, contamination and infec

U.S. FDA — Device Enforcement · Canada · 2016-02-24 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1251-2016
Date of alert: 2016-02-24
Country / jurisdiction: Canada
Risk level: Class II
Risk type: recall
Brand: Amd Ritmed
Product category: device
Product type: Devices

Reported risk: Product does not meet sterility requirements based on FDA analysis and tested positive for Bacterium Bacillus.

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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