3M™ Nexcare™ 432-100Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30051131212764), received between Mar 22, 2021 and Mar 22, 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMar 22, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  A FEMALE CUSTOMER ALLEGED THAT HER 10 YEARS OLD DAUGHTER HAD A SEVERE ALLERGIC REACTION TO THE NEXCARE WATERPROOF BANDAGES. HER DAUGHTER HAD A WART INFECTION. SHE APPLIED AN OVER THE COUNTER WART MEDICINE (MEDICATION UNSPECIFIED) TO THE AREA BEFORE SHE APPLIED THE NEXCARE BANDAGE. ONE BANDAGE WAS APPLIED TO HER RIGHT KNEE AND ANOTHER BANDAGE WAS APPLIED TO HER RIGHT INNER THIGH. SHE USED THE BANDAGE FOR 3 CONSECUTIVE DAYS. THE BANDAGE WAS IN PLACE FOR ABOUT 16-24 HOURS AND WAS CHANGED DAILY. SHE FIRST NOTICED THE ALLEGED INJURY ON (B)(6) 2021. SHE ALLEGED THE AREA WAS RED, BUBBLY AND LOOKED LIKE A BLISTER. SHE TREATED THE AREAS WITH A STEROID CREAM (TRIAMCINOLONE ACETONITE OINTMENT) THAT WAS PRESCRIBED BY THE DOCTOR. THE ALLEGED INJURY IS RESOLVING. SHE REPORTED THAT HER DAUGHTER IS ALLERGIC TO HAY FEVER AND HAD A PAST ALLERGIC REACTION TO LATEX TAPE AFTER ROUTINE INFANT IMMUNIZATION. NO MEDICAL HISTORY REPORTED.

  Patient problems: Blister; Local Reaction; Skin Inflammation/ Irritation

  MAUDE report 11546393 ↗