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

Recall Z-2043-2018 — Medical Action Industries Inc. Blue OR Towel Non X-Ray Detectable (6 Towels per Pack) / product # AVID266 Sterile This OR towel product is intended for external use only. These towels are intended to be used as absorbent towels for hand drying, cleanup, and to provide increased absorbency of bloo

U.S. FDA — Device Enforcement · United States · 2017-12-11 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2043-2018
Date of alert: 2017-12-11
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Medical Action Industries Inc
Product category: device
Product type: Devices

Reported risk: Product sterility potentially compromised.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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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