FDA Adverse Event Injury Summary report: N

ASR ACETABULAR CUPS 52

MDR report key: 2895579 · Received January 3, 2013

Report

Report Number
1818910-2013-00211
Event Type
Injury
Date Received
January 3, 2013
Report Date
December 17, 2012
Manufacturer
DEPUY INTERNATIONAL
Product Code
KWA
PMA / PMN Number
K040627
Removal / Correction Number
Z-1749/1816-2011
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SC, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

DEPUY STILL CONSIDERS THIS INVESTIGATION CLOSED.

Additional Manufacturer Narrative · 1

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.

Description of Event or Problem · 1

LITIGATION ALLEGED THE PATIENT SUFFERED PAIN, DISCOMFORT AND OTHER UNSPECIFIED INJURIES AS A RESULT OF EXCESSIVE LEVELS OF CHROMIUM AND COBALT WITHIN THE IMPLANTED ASR HIP. LEFT HIP. DOI: (B)(6) 2008 - DOR: NONE REPORTED. UPDATE: 5/1/2013 - PLAINTIFF'S PRELIMINARY DISCLOSURE FORM WAS RECEIVED, WHICH IDENTIFIED PART/LOT INFORMATION. THE COMPLAINT AND ASSOCIATED MDRS WERE UPDATED. THERE WAS NO NEW INFORMATION THAT WOULD CHANGE THE OUTCOME OF THE INVESTIGATION.

Description of Event or Problem · 1

LITIGATION ALLEGED THE PATIENT SUFFERED PAIN, DISCOMFORT AND OTHER UNSPECIFIED INJURIES AS A RESULT OF EXCESSIVE LEVELS OF CHROMIUM AND COBALT WITHIN THE IMPLANTED ASR HIP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2799 ASR ACETABULAR CUPS 52 ACETABULAR CUP HIP IMPLANT KWA DEPUY INTERNATIONAL 2538503

Patients

Seq Age Sex Outcome Treatment
1 Other