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

Recall Z-1203-2018 — Johnson & Johnson BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wrap (size: 2in)

U.S. FDA — Device Enforcement · United States · 2017-12-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1203-2018
Date of alert
2017-12-18
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Johnson & Johnson Consumer, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
111615000
Reported risk: Johnson & Johnson Consumer Inc. is initiating a voluntary, Class II recall at the retail level in the U.S. of select COACH¿ Self-Adhering Sports Wraps, BAND-AID¿ Brand First Aid Products SECURE-FLEX¿ Wraps and BAND-AID¿ Brand First Aid Products HURT-FREE¿ Wraps products. The current labeling claim states not made with natural rubber latex which needs to be updated based upon recent awareness that natural latex was used as a base ingredient in the early-stage manufacturing process, which reduces the allergic protein found in natural latex.
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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