TOTAL ASR ACET IMP SIZE 60
Report
- Report Number
- 1818910-2013-00988
- Event Type
- Injury
- Date Received
- January 17, 2013
- Date of Event
- January 12, 2013
- Report Date
- August 12, 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
- PATIENT
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 - RIGHT HIP;REASON FOR REVISION: PAIN.
NEW ETQ RECORD CREATED IN ORDER TO UPDATE ETQ (LEGACY SYSTEM) COMPLAINT NUMBER (B)(4). REASON FOR ORIGINAL COMPLAINT - ASR REVISION DUE TO TAKE PLACE ON (B)(6) 2013, RIGHT, ASR XL, REASON(S) FOR REVISION: PAIN. LOT NUMBER 2256550 FOR STEM INCORRECT. USED INSTEAD 2256660. UPDATE RECEIVED: (B)(6) 2014 - ADDED HOSPITAL: (B)(6) HOSPITAL AND ADDED REVISION DATE TO REVISION DATE FIELD.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 26257 | TOTAL ASR ACET IMP SIZE 60 | HIP ACETABULAR CUP | KWA | DEPUY INTERNATIONAL LTD. 8010379 | 2278889 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |