FDA Adverse Event
Injury
Summary report: N
BHR
MDR report key: 1863419
·
Received October 11, 2010
Report
- Report Number
- 3005477969-2010-00171
- Event Type
- Injury
- Date Received
- October 11, 2010
- Date of Event
- April 12, 2010
- Report Date
- October 11, 2010
- Manufacturer
- SMITH & NEPHEW ORTHOPAEDICS, LTD.
- Product Code
- NXT
- PMA / PMN Number
- P040033
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT REVISION SURGERY WAS PERFORMED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BHR | ACETABULAR CUP | NXT | SMITH & NEPHEW ORTHOPAEDICS, LTD. | 71716 032 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 64 YR | Hospitalization | FEMORAL HEAD, PART#74121146, LOT#74044 036 |