3M™ Ioban™ 6651EZRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30707387793099), received between Jul 20, 2023 and Jul 20, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Human-Device Interface 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 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.

• InjuryJul 20, 2023Human-Device Interface Problem; Human-Device Interface Problem

  REPORT RECEIVED FROM THE FDA VIA MEDWATCH REPORT (B)(4). A RISK MANAGER REPORTED A 76-YEAR-OLD FEMALE ALLEGEDLY EXPERIENCED A LEFT UPPER ARM DIME SIZED SKIN TEAR WITH THE USE OF THE 3M¿ IOBAN¿ 2 ANTIMICROBIAL INCISE DRAPE, 6651EZ. NO MEDICAL TREATMENT WAS REQUIRED TO TREAT THE REPORTEDLY MINOR INJURY, AND FOR PATIENT COMFORT ONLY, AN ALTERNATE DRESSING WAS SUBSEQUENTLY APPLIED IT WAS ALSO NOTED THAT THERE WAS NO DIFFICULTY REMOVING THE 3M¿ IOBAN¿ 2 ANTIMICROBIAL INCISE DRAPE, 6651EZ, AND THE PRODUCT WAS PARTIALLY APPLIED UNDER TENSION.

  Patient problems: Skin Tears

  MAUDE report 17358370 ↗