FDA Adverse Event Injury Summary report: N

LCS COMP RP INSERT STD 10MM

MDR report key: 2060695 · Received April 6, 2011

Report

Report Number
1818910-2011-05757
Event Type
Injury
Date Received
April 6, 2011
Date of Event
March 8, 2011
Report Date
March 8, 2011
Manufacturer
DEPUY ORTHOPAEDICS, INC.
Product Code
NJL
PMA / PMN Number
P830055/S074
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

CORRECTED: LOT #, MANUFACTURE DATE. EXAMINATION OF THE POLYETHYLENE INSERT CONFIRMED ANTICIPATED WEAR FOR A POLYETHYLENE KNEE DEVICE IMPLANTED FOR APPROXIMATELY SEVEN YEARS. A SEARCH OF THE COMPLAINT DATABASE DID NOT SHOW ANY ADDITIONAL REPORTS AGAINST THE LOT CODE. NO EVIDENCE WAS FOUND INDICATING PRODUCT FAILURE OR PRODUCT CONTRIBUTION TO THE REPORTED EVENT AND THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED.

Additional Manufacturer Narrative · 1

THE PRODUCT ASSOCIATED WITH THIS REPORTED EVENT WAS NOT RETURNED FOR EXAMINATION. A SEARCH OF THE COMPLAINT DATABASE DID NOT SHOW ANY ADDITIONAL REPORTS AGAINST THE LOT CODES. THE INVESTIGATION COULD NOT DRAW ANY CONCLUSIONS ABOUT THE REPORTED EVENT WITHOUT THE PRODUCTS TO EXAMINE. NO EVIDENCE WAS FOUND SUGGESTING PRODUCT ERROR WAS A CONTRIBUTING FACTOR AND THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT AND/OR ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED.

Description of Event or Problem · 1

PATIENT REVISED FOR LOOSE FEMORAL, TIBIAL AND PATELLA COMPONENTS AND NOTED OSTEOLYSIS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LCS COMP RP INSERT STD 10MM 87NJL NJL DEPUY ORTHOPAEDICS, INC. NA YP7A54000

Patients

Seq Age Sex Outcome Treatment
1 71 YR Required Intervention