FDA Adverse Event
Injury
Summary report: N
9612771-2007-00001
MDR report key: 808368
·
Received January 9, 2007
Report
- Report Number
- 9612771-2007-00001
- Event Type
- Injury
- Date Received
- January 9, 2007
- Product Code
- JWH
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
AS OF THIS DATE IT HAS BEEN INDICATED THAT THE DEVICE MAY NOT BE RETURNED TO PLUS ORTHOPEDICS USA. SHOULD IT BE RETURNED TO PLUS AT SOME POINT IN THE FUTURE, IT WILL BE FORWARDED TO THE MFR FOR AN EVALUATION. PLUS ORTHOPEDICS USA IS IN THE PROCESS OF OBTAINING ADDITIONAL DETAILS ON THE REVISION SURGERY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | JWH |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |