FDA Adverse Event
Injury
Summary report: N
ASIAN IMHS
MDR report key: 1153310
·
Received September 9, 2008
Report
- Report Number
- 1020279-2008-00233
- Event Type
- Injury
- Date Received
- September 9, 2008
- Date of Event
- July 10, 2008
- Report Date
- August 18, 2008
- Manufacturer
- SMITH & NEPHEW, INC., ORTHOPAEDIC DIV.
- Product Code
- JDS
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- JA
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
NA
Description of Event or Problem · 1
THE PATIENT UNDERWENT REVISION SURGERY DUE TO THE NAIL BREAKING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ASIAN IMHS | INTERNAL FIXATION - NAIL | JDS | SMITH & NEPHEW, INC., ORTHOPAEDIC DIV. | 05CM12955 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK | Other |