DXTEND STAND PE CUP D38 +6MM
Report
- Report Number
- 1818910-2011-00586
- Event Type
- Injury
- Date Received
- January 26, 2011
- Date of Event
- December 27, 2010
- Report Date
- December 27, 2010
- Manufacturer
- DEPUY FRANCE S.A.
- Product Code
- HSD
- PMA / PMN Number
- K062250
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AS
- Reporter Occupation
- OTHER
Narratives
THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.
THE DEVICES ASSOCIATED WITH THIS REPORT WERE NOT RETURNED. A SEARCH OF THE COMPLAINT DATABASE FOUND NO PRIOR REPORTS FOR BOTH OF THE REPORTED PART AND LOT NUMBER COMBINATIONS. A DEPUY FRANCE SUPPLIER REVIEWED THE DEVICE HISTORY RECORDS AND FOUND THE PRODUCTS CONFORMED TO THE REQUIRED SPECIFICATIONS AND FOUND NO MANUFACTURING DEVIATIONS OR ANOMALIES. BASED ON THE INVESTIGATION THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED. SHOULD ANY ADDITIONAL INFORMATION BE RECEIVED TO CHANGE THE OUTCOME OF THE PERFORMED INVESTIGATION, THE COMPLAINT WILL BE RE-OPENED.
PT PRESENTED TO HOSP WITH PAIN AND SWELLING TO SHOULDER. FOLLOWING INVESTIGATIONS, PT DIAGNOSED WITH DEEP TISSUE INFECTION AND PRESCRIBED INTRAVENOUS ANTIBIOTICS. INITIALLY PERFORMED A WOUND WASHOUT WITH LITTLE IMPROVEMENT. ON (B)(6) 2010 - DEVICE EXCHANGE. INFECTED MEMBRANE REMOVED FROM THE UNDERSIDE OF BOTH IMPLANTS AND SENT FOR PATHOLOGY, RESULTS PENDING. THERE WAS NO EVIDENCE OF LOOSE COMPONENTS AS THE TIME OF REVISION SURGERY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DXTEND STAND PE CUP D38 +6MM | 87HSD 87KWS | HSD | DEPUY FRANCE S.A. | NA | 5020715 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 67 YR | Required Intervention |