ASR ACETABULAR IMP 52
Report
- Report Number
- 1818910-2011-15795
- Event Type
- Injury
- Date Received
- August 18, 2011
- Report Date
- July 22, 2011
- Manufacturer
- DEPUY INTERNATIONAL, LTD.
- Product Code
- KWA
- PMA / PMN Number
- NA
- Removal / Correction Number
- Z-1749/1816-2011
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AS
- Reporter Occupation
- OTHER
Narratives
NO 510(K) NUMBER PROVIDED BECAUSE THIS IMPLANT IS SOLD INTERNATIONALLY WITH DIFFERENT INDICATIONS FOR USE; IT IS CURRENTLY SOLD IN THE US UNDER A DIFFERENT PART NUMBER. THE CORRECTION/REMOVAL REPORTING NUMBER LISTED APPLIES TO THE CORRESPONDING PRODUCT CODE SOLD DOMESTICALLY. 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.
THE SUBJECT UNDERWENT PRIMARY TOTAL HIP REPLACEMENT IN (B)(6) 2006 FOR DEVELOPMENTAL DYSPLASIA OF THE HIP. IT WAS REPORTED IN (B)(6) 2011 THAT THE SUBJECT HAD BEEN REVIEWED AND HAD BLOOD METAL ION TESTS AS PART OF THE ASR RECALL AND HAS HIGH COBALT LEVELS. RIGHT HIP. REVISION (B)(6) 2011. A GREY STAINED EFFUSION WAS FOUND WITHIN THE JOINT CAPSULE AND THE SYNOVIUM INSIDE THE CAPSULE WAS STAINED ALSO. THE SILENT HIP WAS NOT REVISED AND REMAINED IN SITU. COBALT LEVELS WERE FOUND TO BE 1500NMOL/L AND CHROMIUM 1000NMOL/L. THE SUBJECT WAS OTHERWISE ASYMPTOMATIC.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ASR ACETABULAR IMP 52 | TOTAL HIP REPLACEMENT | KWA | DEPUY INTERNATIONAL, LTD. | NA | 1900703 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |