3M™ Micropore™ 1533-1Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30707387066018), received between Jun 9, 2021 and Jun 9, 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 16, 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.

• InjuryJun 9, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  RECEIVED FROM (B)(6): A PATIENT HAD AN OPERATION DUE TO UNDERARM ODOR AND 3M¿ MICROPORE¿ SURGICAL TAPE WAS APPLIED AFTER THE PROCEDURE. ABOUT 30 MINUTES LATER, SKIN REDNESS, ITCHINESS, SWELLING AND A FEW BLISTERS RESULTED IN THE TAPE APPLICATION AREA. THE SKIN WAS WIPED WITH ALCOHOL, DEXAMETHASONE WAS GIVEN INTRAVENOUSLY AND APPLIED TOPICALLY TO THE SKIN, AND THE AREA WAS NO LONGER COVERED WITH 3M TAPES AND ELASTIC BANDAGES. AFTER TREATMENT, THE SYMPTOMS WERE ALLEVIATED.

  Patient problems: Erythema; Skin Inflammation/ Irritation

  MAUDE report 11970320 ↗