UNKNOWN DEPUY ASR FEMORAL HEAD
Report
- Report Number
- 1818910-2013-21975
- Event Type
- Injury
- Date Received
- July 24, 2013
- Date of Event
- July 17, 2013
- Report Date
- July 17, 2013
- Manufacturer
- DEPUY INTL., LTD. - 8010379
- Product Code
- KXA
- Removal / Correction Number
- Z-1749/1816-2011
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- ATTORNEY
Narratives
THE 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.
IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED.
LITIGATION RECEIVED ALLEGING THAT THE PATIENT SUFFERS FROM THE ACETABULAR CUP PRODUCING METALLIC DEBRIS, LOOSENING FROM THE ACETABULUM, PAIN, AND ABNORMAL BLOOD METAL ION CONCENTRATIONS. COMMENT: IT SHOULD BE NOTED THAT THE LAW FIRM USES THE SAME (OR SIMILAR) COMPLAINT FOR ALL PATIENTS, SO IT IS POSSIBLE THESE SYMPTOMS ARE NOT SPECIFIC TO THIS PATIENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 344797 | UNKNOWN DEPUY ASR FEMORAL HEAD | FEMORAL HEAD | KXA | DEPUY INTL., LTD. - 8010379 | UNKNOWN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |