SUMMIT POR TAPER SZ4 HI OFF
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
THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.
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.
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 |