FDA Adverse Event Injury Summary report: N

UNKNOWN DEPUY FEMORAL

MDR report key: 2999422 · Received March 12, 2013

Report

Report Number
1818910-2013-04217
Event Type
Injury
Date Received
March 12, 2013
Date of Event
September 5, 2012
Report Date
February 15, 2013
Manufacturer
DEPUY WARSAW
Product Code
JWH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE INVESTIGATION HAS BEEN REOPENED DUE TO RECEIVING INFORMATION ON THE PATELLA AND FEMORAL. DEPUY WILL NOTIFY THE FDA WHEN THE INVESTIGATION IS COMPLETE.

Additional Manufacturer Narrative · 1

UPDATE - (B)(4) 2013 - THE PATIENT'S MEDICAL RECORDS WERE RECEIVED. RECORDS INDICATE UPON REVISION PATELLA BAJA WAS FOUND. THE FEMORAL AND PATELLA WERE ADDED TO THE COMPLAINT AND THE COMPLAINT WAS RE-OPENED. MEDICAL RECORDS AND X-RAYS WERE OBTAINED AND REVIEWED. THE PRODUCT CODE AND LOT CODE REQUIRED IN RETRIEVING THE DEVICE HISTORY RECORDS FOR REVIEWING AND SEARCHING THE COMPLAINT DATABASE FOR THE NEWLY ADDED PRODUCTS WERE NOT PROVIDED. THE INVESTIGATION COULD NOT DRAW ANY CONCLUSIONS REGARDING THE REPORTED EVENT WITH THE PROVIDED INFORMATION. BASED ON THE INABILITY TO IDENTIFY A ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION WAS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ANY ADDITIONAL INFORMATION BE RECEIVED TO CHANGE THE OUTCOME OF THE PERFORMED INVESTIGATION, THE COMPLAINT WILL BE RE-OPENED.

Description of Event or Problem · 1

CLINICAL REPORT STATES: ASEPTIC LOOSENING OF THE TIBIAL TRAY. **UPDATE** (B)(4) 2013 - THE PATIENT'S MEDICAL RECORDS WERE RECEIVED. RECORDS INDICATE UPON REVISION PATELLA BAJA WAS FOUND. THE FEMORAL AND PATELLA WERE ADDED TO THE COMPLAINT AND THE COMPLAINT WAS RE-OPENED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
104275 UNKNOWN DEPUY FEMORAL FEMORAL JWH DEPUY WARSAW UNK

Patients

Seq Age Sex Outcome Treatment
1 56 YR Required Intervention