FDA Adverse Event Injury Summary report: N

T-LINE MESH

MDR report key: 23295423 · Received October 15, 2025

Report

Report Number
MW5177341
Event Type
Injury
Date Received
October 15, 2025
Date of Event
August 8, 2025
Report Date
October 9, 2025
Manufacturer
DEEP BLUE MEDICAL ADVANCES, INC.
Product Code
FTL
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
US
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Description of Event or Problem · 0

ABDOMINAL WALL DEHISCENCE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2471361 T-LINE MESH MESH, SURGICAL, POLYMERIC FTL DEEP BLUE MEDICAL ADVANCES, INC.

Patients

Seq Age Sex Outcome Treatment
1 57 YR Male Hospitalization| R