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

Recall Z-0601-2016 — 3M Coban Self-Adherent Wrap Shipper carton label identified the product as 3M Coban LF Latex Free Catalog #2081, lot number 2018-10AM.

U.S. FDA — Device Enforcement · United States · 2015-12-01 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0601-2016
Date of alert
2015-12-01
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
3M Company - Health Care Business
Product category
device
Product type
Devices
Reported risk: Product mislabeled as latex free. Actual Catalog number 1581, lot 2020-10AN. contains latex. This could pose a health risk to users with sensitivity or allergic reaction to latex, which could range from mild to severe.
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.

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