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

Recall Z-1074-2017 — Unna-Z, Unna Boot with Zinc and Calamine, Compression Wrap, 1 Per Box, 3-4in x 10yds

U.S. FDA — Device Enforcement · United States · 2016-11-23 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1074-2017
Date of alert: 2016-11-23
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Medline Industries Inc
Product category: device
Product type: Devices

Reported risk: Medline Industries, Inc is recalling Unna Z Unna Boot Bandage 3X10 and Unna Z Unna Boot Bandage 4X10 due to contamination of the products with common mold (Cladosporium sphaerospermum/cladosporioides/herbarum/phaenocomae/halotolerans and Penicillium corylophilum)..

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.