FDA Adverse Event
Injury
Summary report: N
BIAX WRIST SMALL METACARPAL LT
MDR report key: 625484
·
Received August 11, 2005
Report
- Report Number
- 1818910-2005-01352
- Event Type
- Injury
- Date Received
- August 11, 2005
- Date of Event
- August 3, 2005
- Report Date
- August 3, 2005
- Manufacturer
- DEPUY ORTHOPAEDICS, INC.
- Product Code
- JWJ
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AZ, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
THE PT WAS REVISED DUE TO METACARPAL COMPONENT LOOSENING AND PAIN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BIAX WRIST SMALL METACARPAL LT | TOTAL WRIST PROSTHESIS | JWJ | DEPUY ORTHOPAEDICS, INC. | NA | WY7G4100 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Required Intervention |