ASR ACETABULAR CUPS 50
Report
- Report Number
- 1818910-2014-28101
- Event Type
- Injury
- Date Received
- September 16, 2014
- Date of Event
- August 29, 2014
- Report Date
- December 10, 2014
- Manufacturer
- DEPUY INTERNATIONAL LTD.-8010379
- Product Code
- KWA
- PMA / PMN Number
- PK040627
- Removal / Correction Number
- Z-1749/1816-2011
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CO, US
- Reporter Occupation
- PHYSICIAN
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 THIS 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.(B)(4). DEPUY STILL CONSIDERS THIS INVESTIGATION CLOSED.
ASR REVISION REPORTED VIA SALES REP; LEFT; REASON(S) FOR REVISION : PAIN / ELEVATED ION LEVELS.
UPDATE REC'D 12/10/2014- LITIGATION PAPERS RECEIVED. LITIGATION ALLEGES PAIN, DISCOMFORT, FLUID ABNORMALITIES, DECREASED RANGE OF MOTION. MUSCLE MASS DETERIORATION OF SOFT TISSUE, AND ELEVATED METAL ION LEVELS. THE DOB WAS PROVIDED. THE STEM IS BEING ADDED BECAUSE OF ELEVATED METAL ION LEVELS. THE COMPLAINT WAS UPDATED ON: 01/27/2014.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 570978 | ASR ACETABULAR CUPS 50 | HIP ACETABULAR CUP | KWA | DEPUY INTERNATIONAL LTD.-8010379 | 2467411 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 73 YR | Required Intervention |