FDA Adverse Event
Summary report: N
MESH
MDR report key: 2935348
·
Received December 31, 2012
Report
- Report Number
- 2935348
- Date Received
- December 31, 2012
- Date of Event
- November 5, 2008
- Report Date
- December 12, 2008
- Product Code
- FTL
- Report Source
- User Facility report
- Reporter Location
- PA, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
PATIENT HAD MESH INSERTION FOR ANTERIOR SUPPORT OF RECURRENT CYSTOCELE AND VAGINAL PROLAPSE. MESH EROSION WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MESH | FTL | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 74 YR |