FDA Adverse Event Injury Summary report: N

ASR ACETABULAR CUPS 50

MDR report key: 2233076 · Received September 2, 2011

Report

Report Number
1818910-2011-17138
Event Type
Injury
Date Received
September 2, 2011
Report Date
August 5, 2011
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
NY, US
Reporter Occupation
ATTORNEY

Narratives

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.

Additional Manufacturer Narrative · 1

DEPUY STILL CONSIDERS THIS INVESTIGATION CLOSED.

Description of Event or Problem · 1

LITIGATION PAPERS ALLEGE THE FOLLOWING: ON OR ABOUT (B)(6) 2010, PATIENT BEGAN SUFFERING DISCOMFORT, PAIN, AND ACHING. HER HIP PAIN CONTINUED TO WORSEN CONSIDERABLY AND SIGNIFICANTLY IMPAIR HER ABILITY TO DRIVE, WORK AND EVEN STAND. IT IS ALSO ALLEGED PATIENT HAS INCREASED METAL IONS LEVELS. UPDATE: 11/14/2011 - THE SALES REP HAS REPORTED THE REVISION SURGERY. PATIENT WAS REVISED DUE TO PAIN.

Description of Event or Problem · 1

LITIGATION PAPERS ALLEGE THE FOLLOWING: ON OR ABOUT (B)(6) 2010, PATIENT BEGAN SUFFRERING DISCOMFORT, PAIN, AND ACHING. HER HIP PAIN CONTINUED TO WORSEN CONSIDERABLY AND SIGNIFICANTLY IMPAIR HER ABILITY TO DRIVE, WORK AND EVEN STAND. IT IS ALSO ALLEGED PATIENT HAS INCREASED METAL IONS LEVELS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ASR ACETABULAR CUPS 50 ACETABULAR CUP KWA DEPUY INTERNATIONAL 2296029

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention