DEPUY ASR XL FEM IMP SIZE 45
Report
- Report Number
- 1818910-2013-05601
- Event Type
- Injury
- Date Received
- May 9, 2013
- Date of Event
- October 21, 2011
- Report Date
- November 2, 2015
- 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. REF. (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 - RIGHT HIP; REASON FOR REVISION: UNKNOWN.
UPDATE 5 NOV. 2015: UPDATED REASON FOR REVISION AS PAIN AND ALVAL / SOFT TISSUE REACTION, ADDED MANUFACTURE AND EXPIRY DATES FOR PRODUCTS, UPDATED FILE HANDLER DETAILS. TAKEN FROM SCF 3 NOV. 2015.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 203141 | DEPUY ASR XL FEM IMP SIZE 45 | HIP FEMORAL HEAD | KWA | DEPUY INTERNATIONAL LTD - 8010379 | 2441585 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |