3M™ Nexcare™ SSB-20ARecalls & reported problems
3M Company · Nexcare™ Sensitive Skin Bandages SSB-20A, Assorted 20 ct · Class 1
All models of 3M Nexcare (10)
Data updated Oct 16, 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 30051131193582), received between Jan 11, 2023 and Jan 11, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (1 report).
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Patient Device Interaction Problem1
Patient problems
- 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.
InjuryJan 11, 2023Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem
A FEMALE CUSTOMER (AGE UNSPECIFIED) REPORTED AN INCIDENT REGARDING THE NEXCARE¿ STRONG HOLD PAIN FREE REMOVAL BANDAGES. ON AN UNSPECIFIED DATE, A MOLE WAS REMOVED FROM HER ABDOMEN. ON (B)(6) 2022, SHE APPLIED THE NEXCARE BANDAGE ON HER ABDOMEN COVERING THE INCISION. THE BANDAGE WAS IN PLACE FOR ABOUT FOUR TO FIVE HOURS. WHILE THE BANDAGE WAS IN PLACE, THE AREA WAS ITCHY. AFTER SHE REMOVED THE BANDAGE, SHE ALLEGEDLY NOTICED A RED LINE WHERE THE BANDAGE PAD WAS PLACED. THE AREA WAS ALLEGEDLY BLOTCHY AND ITCHY. SHE ALLEGED THE REDNESS SPREAD ROUGHLY 5"X10" FROM WHERE THE PAD TOUCHED HER SKIN. THE REDNESS WAS ALLEGEDLY ONLY ON THE RIGHT SIDE OF HER ABDOMEN. ON UNSPECIFIED DATE, SHE SENT THE PICTURES OF THE ALLEGED INJURY TO HER DERMATOLOGIST. THE DERMATOLOGIST PRESCRIBED AN UNSPECIFIED STEROID CREAM. SHE APPLIED THE CREAM TWICE A DAILY AND PLACED ICE ON THE AREA. ON AN UNSPECIFIED DATE, THE INFLAMMATION STARTED TO DECREASE. HER DOCTOR SAID THAT IT WILL BE A WHILE BEFORE THE ALLEGED INJURY COMPLETELY RESOLVED. ON (B)(6) 2023, THE CUSTOMER ALLEGED THE OUTLINE OF THE PAD AND INFLAMED ITCHY AREAS ON HER SKIN WERE STILL VISIBLE AFTER THREE WEEKS OF USING THE PRESCRIBED STEROID CREAM TWICE D
Patient problems: Rash; Skin Inflammation/ Irritation
MAUDE report 16142183 ↗
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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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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