Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ACE(TM) BRAND Recalled by 3M Company - Health Care Business Due to Mold was found on the non-patient contact surfaces...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact 3M Company - Health Care Business directly.
Affected Products
ACE(TM) BRAND, ULTRA LITE ANKLE brace: (a) Size Selection Medium, Cat #901014, UPC 051131019984 2; (b) Size Selection Large, Cat #901015, UPC 0 51131019985 9
Quantity: 996 units
Why Was This Recalled?
Mold was found on the non-patient contact surfaces of the product and was identified as Aspergillus candidus.
Where Was This Sold?
This product was distributed to 32 states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, IL, IN, IA, KS, KY, LA, MD, MI, MS, MO, NH, NY, NC, OH, OR, PA, SC, TN, TX, UT, VA, WV, WI
About 3M Company - Health Care Business
3M Company - Health Care Business has 40 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report