LCS COMPLETE POLY PATELLA STD+
Report
- Report Number
- 1818910-2014-28744
- Event Type
- Injury
- Date Received
- September 24, 2014
- Date of Event
- September 8, 2014
- Report Date
- September 8, 2014
- Manufacturer
- 9616671 DEPUY (IRELAND)
- Product Code
- NJL
- PMA / PMN Number
- PP830055
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MT, US
- Reporter Occupation
- HEALTH PROFESSIONAL
Narratives
ADDITIONAL NARRATIVE: THE DEVICE ASSOCIATED WITH THIS REPORT WAS NOT RETURNED. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY PRODUCT CONTRIBUTION TO THE REPORTED EVENT WITH THE INFORMATION PROVIDED. BASED ON THE INABILITY TO IDENTIFY ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION WAS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY.
(B)(6). 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.
PATIENT WAS REVISED TO ADDRESS POLY WEAR OF THE INSERT DUE TO A BONE SPUR RUBBING ON IT, AN INCORRECTLY ROTATED PATELLA, VALGUS MALPOSITIONING OF THE TIBIAL TRAY, AND OSTEOLYSIS. FEMORAL LOOSENING AT THE CEMENT/BONE INTERFACE WAS ALSO REPORTED. DEPUY CEMENT WAS USED AT THE TIME OF ORIGINAL IMPLANTATION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 596034 | LCS COMPLETE POLY PATELLA STD+ | KNEE PATELLAR COMPONENT | NJL | 9616671 DEPUY (IRELAND) | 2824340 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |