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 |