FDA Adverse Event
Injury
Summary report: N
2936485-2007-00003
MDR report key: 809898
·
Received January 15, 2007
Report
- Report Number
- 2936485-2007-00003
- Event Type
- Injury
- Date Received
- January 15, 2007
- Product Code
- FFZ
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
THE HOSP IS NOT SURE IF IT WAS EVEN A STRYKER DEVICE USED DURING THE PROCEDURE. NO DEVICE WILL BE RETURNED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | FFZ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |