FDA Adverse Event
Injury
Summary report: N
INTERTAN NAIL
MDR report key: 2190052
·
Received August 4, 2011
Report
- Report Number
- 1020279-2011-00298
- Event Type
- Injury
- Date Received
- August 4, 2011
- Date of Event
- July 26, 2011
- Report Date
- August 4, 2011
- Manufacturer
- SMITH & NEPHEW, INC.
- Product Code
- JDS
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT THE NAIL FRACTURED AND A REVISION SURGERY IS BEING PERFORMED TO CORRECT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INTERTAN NAIL | NAIL FIXATION | JDS | SMITH & NEPHEW, INC. | 10KM18267 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |