FDA Adverse Event
Injury
Summary report: N
UNKNOWN ZIMMER TM ANKLE
MDR report key: 4223300
·
Received October 29, 2014
Report
- Report Number
- 1822565-2014-01490
- Event Type
- Injury
- Date Received
- October 29, 2014
- Report Date
- October 1, 2014
- Manufacturer
- ZIMMER, INC.
- Product Code
- HSN
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UT, US
- Reporter Occupation
- PHYSICIAN
Narratives
Additional Manufacturer Narrative · 1
THIS REPORT WILL BE AMENDED WHEN OUR INVESTIGATION IS COMPLETE.
Description of Event or Problem · 1
IT IS REPORTED THAT THE PATIENT IS EXPERIENCING PAIN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 691305 | UNKNOWN ZIMMER TM ANKLE | ANKLE PROSTHESIS | HSN | ZIMMER, INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |