FDA Adverse Event Injury Summary report: N

ASR ACETABULAR CUPS 60

MDR report key: 2220198 · Received August 15, 2011

Report

Report Number
1818910-2011-14583
Event Type
Injury
Date Received
August 15, 2011
Report Date
June 24, 2011
Manufacturer
DEPUY INTL LTD
Product Code
KWA
PMA / PMN Number
K040627
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

THE ASR PLATFORM WAS VOLUNTARILY RECALLED FROM THE MARKET IN (B)(6), 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.

Additional Manufacturer Narrative · 1

THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.

Description of Event or Problem · 1

LITIGATION PAPERS ALLEGE THE PT WAS REVISED DUE TO RECURRENT DISLOCATIONS, THE PT'S ASR CUP AND HEAD WERE REPLACED WITH A NEW ASR CUP AND HEAD ON OR ABOUT (B)(6) 2007. IT IS FURTHER ALLEGED THE PT EXPERIENCED COBALT AND/OR CHROMIUM POISONING, PAIN, CRACKING AND POPPING IN THE LEFT HIP; CONSTANT PAIN, INABILITY TO LEAD A NORMAL LIFE, NUMEROUS F/U DR VISITS, ANXIETY, FEAR AND MENTAL ANGUISH AND OTHER EMOTIONAL AND PHYSICAL DAMAGES. THE PT UNDERWENT EXPLANT SURGERY ON HIS LEFT HIP ON OR ABOUT (B)(6) 2011.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ASR ACETABULAR CUPS 60 87KWA KWA DEPUY INTL LTD NA 2247493

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention