FDA Adverse Event Injury Summary report: N

ASR ACETABULAR CUPS 58

MDR report key: 4133886 · Received October 2, 2014

Report

Report Number
1818910-2014-29247
Event Type
Injury
Date Received
October 2, 2014
Date of Event
September 24, 2014
Report Date
September 24, 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
VA, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

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.

Additional Manufacturer Narrative · 1

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 THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT AND/OR ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED. (B)(4).

Description of Event or Problem · 1

ASR REVISION REPORTED VIA SALES REP.ASR XL.LEFT.LITIGATION PAPERS ALLEGE PAIN, STIFFNESS, DISFIGUREMENT, AND BODILY INJURY.PATIENT HAD HIP REVISION FOR ASR HIP. PT HAS HAD COBALT / CHROMIUM LEVELS AND PAIN. IMPLANTS REMOVED AND NEW CUP, LINER AND HEADBALL IMPLANTED.

Description of Event or Problem · 1

LITIGATION PAPERS ALLEGE PAIN, STIFFNESS, DISFIGUREMENT, AND BODILY INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
614410 ASR ACETABULAR CUPS 58 HIP ACETABULAR CUP KWA DEPUY INTL., LTD. - 8010379 2171132

Patients

Seq Age Sex Outcome Treatment
1 79 YR Other