FDA Adverse Event Injury Summary report: N

TRANSPARENT DRESSING 41N X 4 3/41N

MDR report key: 23751134 · Received December 8, 2025

Report

Report Number
MW5180142
Event Type
Injury
Date Received
December 8, 2025
Date of Event
July 30, 2025
Report Date
July 30, 2025
Manufacturer
3M COMPANY
Product Code
FRO
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
CA, US
Reporter Occupation
PHARMACIST
Health Professional
Yes

Narratives

Description of Event or Problem · 0

REPORT: (B)(4): LLT CODES: 10069327: PRODUCT QUALITY ISSUE, (B)(4): MEDICINAL PATCH ADHESION ISSUE. NARRATIVE: PATIENT REPORTS TEGADERM HAS BEEN INEFFECTIVE AND DOES NOT "STICK WELL." PATIENT FEELS THE QUALITY OF THE TEGADERM HAS REDUCED RECENTLY. FROM 4. DIAGNOSES FOR USE (DRESSING) -; COMPLEX SIG ORDER (PROD 1): SIG: APPLY DRESSING TOPICALLY AS DIRECTED FOR WOUND CARE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2797496 TRANSPARENT DRESSING 41N X 4 3/41N DRESSING, WOUND, DRUG FRO 3M COMPANY

Patients

Seq Age Sex Outcome Treatment
1 67 YR Female