FDA Adverse Event
Injury
Summary report: N
UNKNOWN LEFT ABGII HIP STEM
MDR report key: 2912807
·
Received January 8, 2013
Report
- Report Number
- 9616680-2013-90055
- Event Type
- Injury
- Date Received
- January 8, 2013
- Date of Event
- July 1, 2012
- Report Date
- December 13, 2012
- Manufacturer
- STRYKER ORTHOPAEDICS CORK
- Product Code
- KWY
- PMA / PMN Number
- UNK
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- KY, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
ADDITIONAL INFO HAS BEEN REQUESTED AND IF RECEIVED, WILL BE PROVIDED IN A SUPPLEMENTAL REPORT.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE PT IS EXPERIENCING SHARP PAIN IN HIS HIP JOINT. PT IS REPORTING NO SWELLING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 10264 | UNKNOWN LEFT ABGII HIP STEM | IMPLANT | KWY | STRYKER ORTHOPAEDICS CORK | NA | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 58 YR | Other |