ASR ACETABULAR IMPLANT 50
Report
- Report Number
- 1818910-2013-05135
- Event Type
- Injury
- Date Received
- April 29, 2013
- Date of Event
- June 5, 2011
- Report Date
- March 28, 2014
- Manufacturer
- DEPUY INTERNATIONAL LTD. 8010379
- Product Code
- KWA
- Removal / Correction Number
- Z-1749/1816-2011
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- 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. THE CORRECTION/REMOVAL REPORTING NUMBER LISTED APPLIES TO THE CORRESPONDING PRODUCT CODE SOLD DOMESTICALLY.
IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE. DEPUY STILL CONSIDERS THIS CASE CLOSED TO CAPA.
ASR REVISION; ASR XL - LEFT HIP; REASON FOR REVISION: UNKNOWN.
NEW ETQ RECORD CREATED IN ORDER TO UPDATE ETQ (LEGACY SYSTEM) COMPLAINT NUMBER DINT 27048. REASON FOR ORIGINAL COMPLAINT ¿ ASR REVISION; ASR XL - LEFT; REASON(S) FOR REVISION: UNKNOWN. UPDATE RECEIVED: 28TH MARCH 2014 - ADDED REASON FOR REVISION: COMPONENT LOOSENING - FEMORAL HEAD, ATTACHED SURGEON CONFIRMATION FORM AND ADDED TAPER SLEEVE LOT NUMBER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 184583 | ASR ACETABULAR IMPLANT 50 | ASR TOTAL HIP REPLACEMENT | KWA | DEPUY INTERNATIONAL LTD. 8010379 | 2198932 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |