3M recalls ACE Deluxe Ankle Braces (model 207736) due to missing latex allergy warning labels. Consumers should check for the label and contact 3M for details.
3M discovered that the Futuro" Quick Strap Ankle Brace (Cat. #47736EN) and ACE" Brand Deluxe Ankle brace (Cat. #207736) do not have the correct labeling. The products contain natural latex rubber, but do not include the appropriate caution statement.
3M is recalling ACE Deluxe Ankle Braces (model 207736) because they lack a required latex allergy warning label. This could cause allergic reactions in people sensitive to natural rubber.
These braces contain natural latex rubber but do not have a warning label about latex allergies. Without the label, users might not know they could have an allergic reaction.
People who own or wear ACE Deluxe Ankle Braces (model 207736) are affected. Those with latex allergies are at higher risk of reaction.
Check for the product model number 207736 and UPC 0 51131 20387 7. All lots of this product are included in the recall.
Look for the latex allergy warning label on the product.
The recall does not require stopping use immediately; check for the label first.
The recall does not specify actions for products with the label.
The recall states the product lacks a warning label, so it may not be safe for those with latex allergies.
We’ve drafted a message you can send ACE to request your refund or repair — edit it as you like.
Subject: Recall Z-0946-2018 — ACE ACE Hello, I own a ACE that is covered by recall Z-0946-2018 from ACE. 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.
