FDA Adverse Event Injury Summary report: N

SUMMIT POR TAPER SZ4 HI OFF

MDR report key: 3173784 · Received June 17, 2013

Report

Report Number
1818910-2013-19060
Event Type
Injury
Date Received
June 17, 2013
Date of Event
June 3, 2013
Report Date
June 3, 2013
Manufacturer
DEPUY ORTHOPAEDICS, INC. - 1818910
Product Code
LPH
PMA / PMN Number
PK001991
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
ATTORNEY

Narratives

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.

Additional Manufacturer Narrative · 1

EXAMINATION OF THE REPORTED DEVICE WAS NOT POSSIBLE AS IT WAS NOT RETURNED. A SEARCH OF THE COMPLAINTS DATABASES FINDS NO OTHER REPORTS AGAINST THE PRODUCT AND LOT CODE COMBINATION SINCE ITS RELEASE TO DISTRIBUTION. THE INVESTIGATION CAN DRAW NO CONCLUSION WITH THE INFORMATION PROVIDED. BASED ON THE INABILITY TO DETERMINE ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION HAS NOT BEEN INDICATED. 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 ALLEGES THAT THE ASR RIGHT HIP IMPLANT CAUSED PAIN IN THE PATIENT. LITIGATION FURTHER ALLEGES THAT THE PATIENT SUFFERED DISABILITY, PHYSICAL IMPAIRMENT, AND DISFIGUREMENT. LITIGATION FURTHER ALLEGES THAT THE PATIENT WAS INJURED BY EXCESSIVE LEVELS OF CHROMIUM AND COBALT IN HER BLOOD AS DETERMINED FROM BLOOD TESTS. SALES REP REPORTED REVISION SURGERY ON RIGHT HIP DUE TO METAL CORROSION ON TRUNION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
273257 SUMMIT POR TAPER SZ4 HI OFF FEMORAL STEM LPH DEPUY ORTHOPAEDICS, INC. - 1818910 BH4D51000

Patients

Seq Age Sex Outcome Treatment
1 75 YR Required Intervention