FDA Adverse Event Injury Summary report: N

LCS COMPLETE POLY PATELLA STD

MDR report key: 3896307 · Received June 26, 2014

Report

Report Number
1818910-2014-22070
Event Type
Injury
Date Received
June 26, 2014
Date of Event
June 6, 2014
Report Date
June 6, 2014
Manufacturer
DEPUY IRELAND 9616671
Product Code
NJL
PMA / PMN Number
PP830055
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
DE, US
Reporter Occupation
PHYSICIAN

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. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

Additional Manufacturer Narrative · 1

THE DEVICE ASSOCIATED WITH THIS REPORT WAS NOT RETURNED. A COMPLAINT DATABASE SEARCH FINDS NO OTHER REPORTED INCIDENTS AGAINST THE PROVIDED PRODUCT AND LOT COMBINATION. REQUESTS FOR ADDITIONAL INVESTIGATIONAL INPUTS WERE MADE IN ACCORDANCE WITH (B)(4) APPENDIX A. NO ADDITIONAL INFORMATION WAS OBTAINED. 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 ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY.

Description of Event or Problem · 1

PATIENT WAS REVISED BECAUSE OF TIBIAL SUBSIDENCE AND OSTEOLYSIS. BONE/CEMENT LOOSENING WAS ALSO NOTED; HOWEVER, IT IS NOT THE SUBJECT OF THE COMPLAINT BECAUSE THE CEMENT WAS MANUFACTURED BY A COMPETITOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
374385 LCS COMPLETE POLY PATELLA STD KNEE PATELLAR COMPONENT NJL DEPUY IRELAND 9616671 3117578

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention