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.
Take action
Contact the company
📍Recalling firm3M Company - Health Care Business3m Center 2510 Conway Ave , B# 275-5-W-6 · Saint Paul, MN 55144-0001
“ACE Deluxe Ankle Brace Recall: Missing Latex Warning Label.” GovInfoNow, updated August 31, 2026. https://govinfonow.com/recall/72068-ace-deluxe-ankle-brace-recall-missing-latex-warning-label. Based on FDA recall #Z-0946-2018 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0946-2018%22&limit=1).
The FDA announced on Jan. 31, 2018, that 3M Company - Health Care Business voluntarily recalled ACE Brand Deluxe Ankle Brace (Cat. #207736) because the products contain natural latex rubber but lack the required caution statement.
How to tell if you have it
ACE(TM) BRAND, DELUXE ANKLE BRACE, 207736
UPC 0 51131 20387 7
The hazard
The products contain natural latex rubber but do not include the appropriate caution statement, according to the FDA.
Context
GovInfoNow's records show 3M Company - Health Care Business has 17 other recalls on record since 2015-08-06. Other recent recalls of similar products include Stryker NICO Myriad Handpieces Recall (2025-10-31), Halyard DAVINCI TRUCUSTOM BUNDLE with natural rubber latex labeling issue (2026-07-09) and AVID Medical Halyard TOTAL JOINT Recall (2026-07-09).
How to tell if you have this one
Check for the product model number 207736 and UPC 0 51131 20387 7. All lots of this product are included in the recall.
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
Distribution
US and Australia, Jordan, Republic Of Korea, Lebanon, New Zealand, Oman, Qatar, Taiwan, United Arab Emirates
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.
Official source: FDA Recall #Z-0946-2018 (January 31, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0946-2018 to see it in context.
Plain-language summary written by qwen3:4b on August 31, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.