Johnson & Johnson recalls 1in HURT-FREE Wraps due to potential natural latex allergy from early manufacturing. Affected products contain trace natural latex that may cause allergic reactions. Consumers should check product codes and contact Johnson & Johnson for details.
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.
Johnson & Johnson is recalling 1-inch HURT-FREE Wraps because they contain trace natural latex from early production. This could cause allergic reactions in sensitive individuals, especially those with latex allergies.
The wraps were manufactured with natural latex in early production stages, which may leave trace amounts of the protein that causes allergies. This risk is low but could affect sensitive individuals.
People who own or use the recalled 1-inch HURT-FREE Wraps are affected. Those with known latex allergies are at higher risk of allergic reactions.
Check for product codes 111614500, 381371161454, or 10381371161451 on the wrap packaging. The product is a 1-inch size.
Look for the product codes 111614500, 381371161454, or 10381371161451 on the wrap packaging.
Johnson & Johnson is recalling these wraps because they contain trace natural latex from early manufacturing, which may cause allergic reactions in sensitive individuals.
No, but people with latex allergies should avoid using them. The recall is for safety, not a stop-use order.
Check the product codes on the packaging: 111614500, 381371161454, or 10381371161451.
We’ve drafted a message you can send Johnson & Johnson to request your refund or repair — edit it as you like.
Subject: Recall Z-1205-2018 — Johnson & Johnson Johnson & Johnson Hello, I own a Johnson & Johnson that is covered by recall Z-1205-2018 from Johnson & Johnson. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
