FDA Adverse Event
Injury
Summary report: N
AVAULTA BIOSYNTHETIC SUPPORT SYSTEM
MDR report key: 2822823
·
Received August 5, 2009
Report
- Report Number
- 1018233-2009-00092
- Event Type
- Injury
- Date Received
- August 5, 2009
- Report Date
- August 5, 2009
- Manufacturer
- SOFRADIM PRODUCTION
- Product Code
- FTL
- Adverse Event
- Yes
- Report Source
- Distributor report
- Reporter Location
- WV, US
- Reporter Occupation
- ATTORNEY
Narratives
Description of Event or Problem · 1
IT WAS ALLEGED BY THE PT'S ATTORNEY FOLLOWING AN ANTERIOR REPAIR AND A POSTERIOR REPAIR PERFORMED IN 2007, "THE PT EXPERIENCED MENTAL AND PHYSICAL PAIN AND SUFFERING, PERMANENT INJURY, PHYSICAL DEFORMITY, LOSS OF A BODILY ORGAN SYSTEM AND HAS UNDERGONE OR WILL UNDERGO CORRECTIVE SURGERY OR SURGERIES". THE PT'S ATTORNEY PROVIDED THE PT'S IMPLANT CARD. THE DIAGNOSIS AND TYPE OF TREATMENT FOR THIS SPECIFIC PT IS NOT KNOWN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | AVAULTA BIOSYNTHETIC SUPPORT SYSTEM | FTL | FTL | SOFRADIM PRODUCTION | NA | ZGK00107 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 53 YR | Required Intervention |