FDA Adverse Event
Injury
Summary report: N
BHR
MDR report key: 2161137
·
Received July 13, 2011
Report
- Report Number
- 3005477969-2011-00146
- Event Type
- Injury
- Date Received
- July 13, 2011
- Date of Event
- April 28, 2010
- Report Date
- September 19, 2011
- Manufacturer
- SMITH & NEPHEW ORTHOPAEDICS, LTD.
- Product Code
- NXT
- PMA / PMN Number
- P040033
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FI
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THAT REVISION SURGERY WAS PERFORMED DUE TO PAIN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BHR | ACETABULAR CUP | NXT | SMITH & NEPHEW ORTHOPAEDICS, LTD. | 17690 083 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| R | FEMORAL HEAD: PART # 74121146, LOT # 29067 010 |