3M™ Coban™ 2083SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00707387802325), received between Aug 29, 2023 and Aug 29, 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 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.

• InjuryAug 29, 2023Human-Device Interface Problem; Human-Device Interface Problem

  A MALE CUSTOMER ALLEGEDLY EXPERIENCED A LEFT ARM ITCHING/BURNING SENSATION, ERYTHEMA, BUMPS, BLISTERING APPROXIMATELY 1/8" WITH SWELLING THIRTY MINUTES POST APPLICATION OF 3M¿ COBAN¿ NL NON-LATEX SELF-ADHERENT WRAP, 2083-1X, LOT# 3MPMDJ. THE PHYSICIAN ADMINISTERED AN ANTIHISTAMINE (NAME UNKNOWN) AND PRESCRIBED TRIAMCINOLONE ACETONIDE 0.1% CREAM. MOST OF THE SYMPTOMS HAVE REPORTEDLY RESOLVED ALTHOUGH THE AREA IS STILL RED, AND THE CUSTOMER CONTINUES TO APPLY THE TOPICAL CREAM. THE CUSTOMER REPORTEDLY HAS NO HISTORY OF ALLERGIES TO TAPES OR OTHER DRESSINGS, AND CONFIRMED THERE IS NO INFECTION PRESENT.

  Patient problems: Blister; Erythema; Itching Sensation

  MAUDE report 17645042 ↗