TOTAL HIP BALL 32MM +11
Report
- Report Number
- 1818910-2014-23738
- Event Type
- Injury
- Date Received
- July 18, 2014
- Date of Event
- September 22, 2009
- Report Date
- June 24, 2014
- Manufacturer
- DEPUY ORTHOPAEDICS, INC.
- Product Code
- JDI
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- PHYSICIAN
Narratives
THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.
THE DEVICES ASSOCIATED WITH THIS REPORT WERE NOT RETURNED. REVIEW OF THE DEVICE HISTORY RECORDS AND/OR A LOT SPECIFIC COMPLAINT DATABASE SEARCH WAS NOT POSSIBLE AS THE LOT CODES REQUIRED WERE NOT PROVIDED. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY PRODUCT CONTRIBUTION TO THE REPORTED EVENT WITH THE INFORMATION PROVIDED. BASED ON THE INABILITY TO IDENTIFY ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION WAS NOT INDICATED.DEPUY CONSIDERS THE INVESTIGATION CLOSED. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY.
CLINICAL REPORT STATES THAT PATIENT UNDERWENT AN OPEN REDUCTION AFTER A FAILED CLOSED REDUCTION ATTEMPT 2.2 YEARS AFTER LINER AND HEAD EXCHANGE FOR FRACTURE OF ACS LINER. ALSO, LINER FRACTURE WAS NOTED DURING THE OPEN REDUCTION AND REVISION WAS SUBSEQUENTLY PERFORMED THE NEXT DAY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 422667 | TOTAL HIP BALL 32MM +11 | HIP FEMORAL HEAD | JDI | DEPUY ORTHOPAEDICS, INC. | K853655 | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |