FDA Adverse Event
Injury
Summary report: N
BHR
MDR report key: 2091538
·
Received May 17, 2011
Report
- Report Number
- 3005477969-2011-00104
- Event Type
- Injury
- Date Received
- May 17, 2011
- Report Date
- May 17, 2011
- 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
Narratives
Description of Event or Problem · 1
IT WAS IDENTIFIED THAT A REVISION SURGERY WAS PERFORMED IN (B)(6) 2010.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BHR | ACETABULAR CUP | NXT | SMITH & NEPHEW ORTHOPAEDICS, LTD. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 54 YR | Hospitalization| R | FEMORAL HEAD, PART AND LOT UNKNOWN |