ASR UNI FEMORAL IMPL SIZE 45
Report
- Report Number
- 1818910-2011-09789
- Event Type
- Injury
- Date Received
- June 3, 2011
- Report Date
- May 4, 2011
- Manufacturer
- DEPUY INTERNATIONAL, LTD.
- Product Code
- KXA
- PMA / PMN Number
- K040627
- Removal / Correction Number
- Z-1749/1816-2011
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- ATTORNEY
Narratives
THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.
DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED.
ASR PLATFORM WAS VOLUNTARILY RECALLED FROM THE MARKET IN AUGUST 2010, AND THE ASR PRODUCT CODES ARE NOW CONSIDERED INACTIVE. FURTHER INVESTIGATION OF THIS INDIVIDUAL INCIDENT WILL NOT BE UNDERTAKEN, AS THERE IS AN ONGOING INVESTIGATION REGARDING THE ROOT CAUSE(S) AND/OR CORRECTIVE ACTIONS. (B)(4).DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT AND/OR ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED.
LITIGATION PAPERS ALLEGE: ON OR ABOUT (B)(6) 2009, PT WAS IMPLANTED WITH A DEPUY ASR XL HIP ON HER RIGHT SIDE. SINCE THE SURGICAL IMPLANTATION, PT HAS EXPERIENCED SYMPTOMS INCLUDING BUT NOT LIMITED TO GROIN PAIN, HIP PAIN, ELEVATED LEVELS OF METAL IONS AND PROBLEMS SITTING, STANDING AND MOVING UP AND DOWN STAIRS. ADDITIONALLY, IT IS ALLEGED THAT PT NOW FACES THE POTENTIAL FOR A REVISION SURGERY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ASR UNI FEMORAL IMPL SIZE 45 | KWA | KXA | DEPUY INTERNATIONAL, LTD. | NA | 2929033 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 72 YR | Required Intervention |