PINN CAN BONE SCREW 6.5MMX25MM
Report
- Report Number
- 1818910-2014-31811
- Event Type
- Injury
- Date Received
- November 17, 2014
- Date of Event
- September 24, 2012
- Report Date
- April 26, 2013
- Manufacturer
- DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS ¿ REG.
- Product Code
- NDJ
- PMA / PMN Number
- PK983014
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- 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. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.
PPD AND MEDICAL RECORDS RECEIVED. THIS COMPLAINT IS LEGAL. PPD ALLEGES INFECTION, BUT AFTER READING THE REVISION OPERATIVE NOTE IT INDICATED PAIN, DISCOMFORT, LOOSE/MALPOSITIONED CUP, AND CYST AROUND THE GREATER TROCHANTER. EXAMINATION OF THE REPORTED DEVICES WAS NOT POSSIBLE AS THEY WERE NOT RETURNED. A SEARCH OF THE COMPLAINTS DATABASES FINDS NO OTHER REPORTS AGAINST THE PRODUCT AND LOT CODE COMBINATIONS SINCE THEIR 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.
PPD AND MEDICAL RECORDS RECEIVED. THIS COMPLAINT IS LEGAL. PPD ALLEGES INFECTION, BUT AFTER READING THE REVISION OPERATIVE NOTE IT INDICATED PAIN, DISCOMFORT, LOOSE/MALPOSITIONED CUP, AND CYST AROUND THE GREATER TROCHANTER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 742465 | PINN CAN BONE SCREW 6.5MMX25MM | HIP OTHER IMPLANT: SCREW | NDJ | DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS ¿ REG. | 421799 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 60 YR | Required Intervention |