FUTURO™ 71060ENRecalls & reported problems
3M Company · FUTURO™ Ultra Sheer Knee Highs for Women Nude 71060EN, Medium · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30051131215901), received between May 20, 2021 and May 20, 2021 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Pain1
- Rash1
- Skin Inflammation/ Irritation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 20, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A FEMALE CUSTOMER (AGE UNSPECIFIED) ALLEGED THE FUTURO¿ ULTRA SHEER KNEE CAUSED A RAISED, RED, ITCHY RASH ALL OVER HER BODY (EXCEPT FOR HER FACE AND BACK) AFTER 2 WEEKS OF USE. SHE PURCHASED THE PRODUCT IN (B)(6) 2021. SHE WORE THE PRODUCT FROM 6AM TO 10 PM DAILY FOR ABOUT 2 WEEKS. DURING THE TWO WEEKS PERIOD SHE WORE THE PRODUCT, SHE RINSED THE PRODUCT, BUT SHE DID NOT WASH WITH SOAP. SHE ALLEGED SHE HAD DIFFICULTY SLEEPING BECAUSE THE ITCHING WAS VERY BAD. HER DOCTOR PRESCRIBED MEDROL FOR ITCHING (DATE UNSPECIFIED). THE ALLEGED INJURY RESOLVED 5 DAYS AFTER SHE STARTED USING THE PRESCRIBED MEDICATION. SHE REPORTED THAT 1.5 YEARS AGO SHE HAD A SIMILAR TYPE OF BODY RASH AFTER SHE UNDERWENT A HIP REPLACEMENT SURGERY (THE DOCTOR USED ADHESIVE SUTURES TO CLOSE THE INCISION). NO ALLERGIES OR MEDICAL HISTORY REPORTED.
Patient problems: Pain; Rash; Skin Inflammation/ Irritation
MAUDE report 11860233 ↗
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- Truform® 0868BL-MSurgical Appliance Industries, Inc. · Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)1 recall0 reports
- Truform® 0868BL-XLSurgical Appliance Industries, Inc. · Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)1 recall0 reports
- Truform® 8846-SSurgical Appliance Industries, Inc. · Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)1 recall0 reports
- Truform® 1756-MSurgical Appliance Industries, Inc. · Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)1 recall0 reports
- Truform® 0866-XLSurgical Appliance Industries, Inc. · Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)1 recall0 reports
- Truform® 8868BL-XLSurgical Appliance Industries, Inc. · Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)1 recall0 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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