FDA Adverse Event Injury Summary report: N

LCS COMPLETE POLY PATELLA STD+

MDR report key: 4112862 · Received September 24, 2014

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 Manufacturer Narrative · 1

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.

Additional Manufacturer Narrative · 1

(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.

Description of Event or Problem · 1

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