FDA Adverse Event
Injury
Summary report: N
AVAULTA POSTERIOR BIOSYNTHETIC SUPPORT SYSTEM
MDR report key: 3203737
·
Received March 26, 2013
Report
- Report Number
- 1018233-2013-00869
- Event Type
- Injury
- Date Received
- March 26, 2013
- Report Date
- February 25, 2013
- Manufacturer
- SOFRADIM PRODUCTION
- Product Code
- FTL
- Adverse Event
- Yes
- Report Source
- Distributor report
- Reporter Location
- GA, US
- Reporter Occupation
- ATTORNEY
Narratives
Description of Event or Problem · 1
THE PT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. ADDITIONAL INFO HAS BEEN REQUESTED, BUT NOT YET RECEIVED. ASSOCIATED MDR 1018233-2013-00870.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 125410 | AVAULTA POSTERIOR BIOSYNTHETIC SUPPORT SYSTEM | FTL | SOFRADIM PRODUCTION | NA | PFG00395 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 50 YR | Required Intervention | PELVILACE TO BIOURETHRAL SUPPORT SYSTEM |