FDA Adverse Event
Injury
Summary report: N
IMHS CP NAIL
MDR report key: 2884017
·
Received December 21, 2012
Report
- Report Number
- 8010764-2012-00055
- Event Type
- Injury
- Date Received
- December 21, 2012
- Date of Event
- September 11, 2012
- Report Date
- September 11, 2012
- Manufacturer
- SMITH & NEPHEW, INC.
- Product Code
- JDS
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
.
Description of Event or Problem · 1
IT WAS REPORTED A REVISION SURGERY WAS PERFORMED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | IMHS CP NAIL | 130 D 10 X 19.5L | JDS | SMITH & NEPHEW, INC. | 12ET19106 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| R | (B)(4) LOT 12DT17215| CHS LAG SC 80MM 3.15 |