FDA Adverse Event
Injury
Summary report: N
TRI TS BASEPLATE SIZE 3
MDR report key: 2171307
·
Received July 15, 2011
Report
- Report Number
- 2249697-2011-01068
- Event Type
- Injury
- Date Received
- July 15, 2011
- Date of Event
- June 22, 2011
- Report Date
- June 22, 2011
- Manufacturer
- STRYKER ORTHOPAEDICS MAHWAH
- Product Code
- JWH
- PMA / PMN Number
- K053514
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
AN EVALUATION OF THE DEVICE CANNOT BE PERFORMED AS THE DEVICE WAS RETAINED BY THE PATIENT AND WAS NOT RETURNED TO THE MANUFACTURER. ADDITIONAL INFORMATION (INCLUDING X-RAYS AND MEDICAL RECORDS) IS NOT AVAILABLE DUE TO HOSPITAL POLICY. IF DEVICE OR ADDITIONAL INFORMATION BECOMES AVAILABLE, THE EVALUATION SUMMARY WILL BE SUBMITTED IN A SUPPLEMENTAL REPORT.
Description of Event or Problem · 1
IT WAS REPORTED THAT, "PATIENT FELL. THE DOCTOR REMOVED THE BASEPLATE AND PROCEEDED TO STEMMED UNIVERSAL BASEPLATE WITH TS POLY. THIS ADDRESSED LIGAMENT STABILITY."
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TRI TS BASEPLATE SIZE 3 | IMPLANT | JWH | STRYKER ORTHOPAEDICS MAHWAH | NA | ULCBA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 78 YR | Required Intervention |