FDA Adverse Event
Injury
Summary report: N
AEQUALIS RESURFACING HEAD
MDR report key: 6202019
·
Received December 23, 2016
Report
- Report Number
- 3000931034-2016-00230
- Event Type
- Injury
- Date Received
- December 23, 2016
- Date of Event
- November 23, 2016
- Report Date
- December 1, 2016
- Manufacturer
- TORNIER S.A.S.
- Product Code
- HSD
- UDI-DI
- 03700386926945
- PMA / PMN Number
- K131231
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THIS IS THE FINAL REPORT SUBMITTED REGARDING THIS SURGICAL EVENT AND MEDICAL DEVICE.
Description of Event or Problem · 1
IT WAS REPORTED THAT A PATIENT UNDERWENT A REVISION SURGERY DUE TO MALPOSITION. CONVERSION TO TSA.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 851782 | AEQUALIS RESURFACING HEAD | HUMERAL RESURFACING | HSD | TORNIER S.A.S. | 43X16 | 03700386926945 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 59 YR | Other |