ASR ACETABULAR CUPS 56
Report
- Report Number
- 1818910-2014-20360
- Event Type
- Injury
- Date Received
- June 5, 2014
- Date of Event
- June 11, 2014
- Report Date
- June 11, 2014
- Manufacturer
- DEPUY INTL., 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
- MN, US
- Reporter Occupation
- ATTORNEY
Narratives
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 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. REF. (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.
LITIGATION ALLEGES PARTIAL LOSS OF MOBILITY AND RANGE OF MOTION AND PAIN. (REVISION SCHEDULED FOR (B)(6) 2014).
UPDATE REC'D 06/11/2014 - DER, IMPLANT MEDICAL RECORDS AND X-RAYS RECEIVED. PATIENT REVISED TO ADDRESS PAIN AND ELEVATED METAL ION LEVELS. THE ADAPTER SLEEVE IS BEING ADDED TO THE COMPLAINT FOR PAIN. THIS COMPLAINT WAS UPDATED ON: 06/25/2014.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 329095 | ASR ACETABULAR CUPS 56 | HIP ACETABULAR CUP | KWA | DEPUY INTL., LTD - 8010379 | 1979833 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 64 YR | Other| R |