TOTAL ASR ACET IMP SIZE 54
Report
- Report Number
- 1818910-2012-76141
- Event Type
- Injury
- Date Received
- October 10, 2012
- Date of Event
- June 26, 2012
- Report Date
- March 26, 2014
- Manufacturer
- DEPUY INTERNATIONAL
- Product Code
- KWA
- Removal / Correction Number
- Z-1749/1816-2011
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- PATIENT
Narratives
DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.
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.
ASR REVISION; LEFT ASR HIP RESURFACING; REASON FOR REVISION: ALVAL/SOFT TISSUE REACTION; PAIN.
NEW ETQ RECORD CREATED IN ORDER TO UPDATE ETQ (LEGACY SYSTEM) (B)(4). REASON FOR ORIGINAL COMPLAINT: ASR REVISION, LEFT, ASR HIP RESURFACING, REASON(S) FOR REVISION: ALVAL / SOFT TISSUE REACTION & PAIN. UPDATE RECEIVED: 26TH MARCH 2014 - ADDED FURTHER REASON(S) FOR REVISION: ENORMOUSLY RAISED METAL IONS AND LYSIS AND ATTACHED SURGEON CONFIRMATION FORM.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TOTAL ASR ACET IMP SIZE 54 | HIP ACETABULAR CUP | KWA | DEPUY INTERNATIONAL | 2568297 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |