FDA Adverse Event Other Summary report: N

ETHILON SUTURE 3-0

MDR report key: 19607487 · Received June 24, 2024

Report

Report Number
MW5156559
Event Type
Other
Date Received
June 24, 2024
Report Date
June 20, 2024
Manufacturer
ETHICON, INC.
Product Code
GAR
Report Source
Voluntary report
Reporter Location
US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Description of Event or Problem · 0

WHITE POWDER/FILM APPEARED ON SUTURE AFTER PASSING THROUGH TISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
626076 ETHILON SUTURE 3-0 SUTURE, NONABSORBABLE, SYNTHETIC, POLYAMIDE GAR ETHICON, INC. THBCSE

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown