FDA Adverse Event
Injury
Summary report: N
HUNTER TENDON ROD
MDR report key: 1338242
·
Received March 5, 2009
Report
- Report Number
- MW5010237
- Event Type
- Injury
- Date Received
- March 5, 2009
- Date of Event
- September 4, 2008
- Report Date
- March 5, 2009
- Manufacturer
- WRIGHT MEDICAL TECHNOLOGY
- Product Code
- HXA
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- IL, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
MD REMOVED HUNTER TENDON ROD- STATED FAILURE OF DEVICE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HUNTER TENDON ROD | HUNTER TENDON ROD | HXA | WRIGHT MEDICAL TECHNOLOGY |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 27 YR | Disability |