FDA Adverse Event Injury Summary report: N

LEAVE ACTIVE PFC STB 10MM SZ5

MDR report key: 2926048 · Received January 23, 2013

Report

Report Number
1818910-2013-11348
Event Type
Injury
Date Received
January 23, 2013
Date of Event
January 15, 2013
Report Date
January 15, 2013
Manufacturer
DEPUY ORTHOPAEDICS, INC.
Product Code
JWH
PMA / PMN Number
PK882234
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MO, 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.

Additional Manufacturer Narrative · 1

THE DEVICE ASSOCIATED WITH THIS REPORT WAS NOT RETURNED. REVIEW OF THE DEVICE HISTORY RECORDS AND/OR A LOT SPECIFIC COMPLAINT DATABASE SEARCH WAS NOT POSSIBLE AS THE LOT CODE REQUIRED WAS NOT PROVIDED. REQUESTS FOR ADDITIONAL INVESTIGATIONAL INPUTS WERE MADE IN ACCORDANCE WITH WI-7915 APPENDIX A; REV. C. NO ADDITIONAL INFORMATION WAS OBTAINED. THE INVESTIGATION COULD NOT DRAW ANY CONCLUSIONS REGARDING THE REPORTED EVENT BASED INSUFFICIENT INFORMATION; HOWEVER, WEAR OF A (B)(4) KNEE DEVICE AFTER BEING IMPLANTED FOR APPROXIMATELY EIGHTEEN YEARS SHOULD NOT BE UNEXPECTED. BASED ON THE INABILITY TO DETERMINE A ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION WAS 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 WAS REVISED TO ADDRESS OSTEOLYSIS AND MEDIAL POLY WEAR OF THE INSERT, WHICH HAD WORN THROUGH.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
32470 LEAVE ACTIVE PFC STB 10MM SZ5 KNEE REPLACEMENT JWH DEPUY ORTHOPAEDICS, INC. UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 84 YR Required Intervention