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

Recall Z-0734-2016 — MediChoice Cohesive Bandages, One (1) roll of cohesive bandage per bag, thirty-six (36) bags per case [all model numbers have equivalent packaging] General Hospital Use.

U.S. FDA — Device Enforcement · United States · 2015-11-17 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0734-2016
Date of alert: 2015-11-17
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Owens & Minor Distribution, Inc.
Product category: device
Product type: Devices

Reported risk: MediChoice sterile cohesive bandages imported and sold under a private brand by Owens & Minor were tested and found to have microbial contamination.

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.

Recall Z-0734-2016 — MediChoice Cohesive Bandages, One (1) roll of cohesive bandage per bag, thirty-six (36) bags per case [all model numbers have equivalent packaging] General Hospital Use.

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