FDA Adverse Event Injury Summary report: N

ASR ACETABULAR CUPS 58

MDR report key: 2990334 · Received March 5, 2013

Report

Report Number
1818910-2013-04231
Event Type
Injury
Date Received
March 5, 2013
Report Date
August 29, 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
GA, 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. REF. (B)(4).

Additional Manufacturer Narrative · 1

MANUFACTURER REGISTRATION #: (B)(4). 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.

Description of Event or Problem · 1

LITIGATION PAPERS ALLEGE PATIENT SUFFERED INJURIES THAT ARE ONGOING AND CONTINUING IN NATURE; EXCESSIVE LEVELS OF COBALT AND CHROMIUM. **UPDATE** - 10/19/2012 - PATIENTS PRELIMINARY DISCLOSURE RECEIVED, WHICH INCLUDED OPERATIVE REPORT OF PRIMARY SURGERY. PRIMARY SURGERY OPERATIVE REPORT STATES THERE WAS AN INTRAOPERATIVE PROXIMAL FEMORAL AND GREATER TROCHANTERIC FRACTURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
94099 ASR ACETABULAR CUPS 58 ACETABULAR CUP KWA DEPUY INTERNATIONAL 1968922

Patients

Seq Age Sex Outcome Treatment
1 Other