RecallDepth

Johnson & Johnson BAND-AID Brand First Aid Products SECURE-FLEX Wrap (size: 3in)

Company
Johnson & Johnson Consumer, Inc.
Recall Initiated
December 18, 2017
Posted
March 27, 2018
Terminated
April 14, 2020
Recall Number
Z-1204-2018
Firm Location
Skillman, NJ

Reason for Recall

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.

Distribution

Nationally

Lot / Code Info

111615100 381371161515 103813711615120000

Root Cause

Labeling design

Action Taken

On December 18, 2017 an URGENT MEDICAL DEVICE RECALL letter was issued to retailers and warehouses with intentions to notify all affected individuals, including customers of the recall. The recall letter requests that the following actions be taken: 1. Immediately examine your inventory and quarantine the above-mentioned product subject to recall. In addition, if you may have further distributed this product to retailers, warehouses or distributors, please identify and send a list of these locations to Stericycle at BandAid8687@stericycle.com and they will be notified. 2. Please complete the enclosed Business Reply Form and return immediately by emailing to BandAid8687@stericycle.com or faxing to (1-888-965-5802). 3. If you have any questions regarding the form, please call Stericycle at (1-855-215-5023). Please return ALL inventory of the identified product above. No product other than that specified is to be returned. Questions or concerns can be directed to 1-855-215-5023

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