FDA Adverse Event Injury Summary report: N

TOTAL HIP BALL 32MM +11

MDR report key: 3943468 · Received July 18, 2014

Report

Report Number
1818910-2014-23738
Event Type
Injury
Date Received
July 18, 2014
Date of Event
September 22, 2009
Report Date
June 24, 2014
Manufacturer
DEPUY ORTHOPAEDICS, INC.
Product Code
JDI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
VA, 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 DEVICES ASSOCIATED WITH THIS REPORT WERE NOT RETURNED. REVIEW OF THE DEVICE HISTORY RECORDS AND/OR A LOT SPECIFIC COMPLAINT DATABASE SEARCH WAS NOT POSSIBLE AS THE LOT CODES REQUIRED WERE NOT PROVIDED. 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. 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

CLINICAL REPORT STATES THAT PATIENT UNDERWENT AN OPEN REDUCTION AFTER A FAILED CLOSED REDUCTION ATTEMPT 2.2 YEARS AFTER LINER AND HEAD EXCHANGE FOR FRACTURE OF ACS LINER. ALSO, LINER FRACTURE WAS NOTED DURING THE OPEN REDUCTION AND REVISION WAS SUBSEQUENTLY PERFORMED THE NEXT DAY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
422667 TOTAL HIP BALL 32MM +11 HIP FEMORAL HEAD JDI DEPUY ORTHOPAEDICS, INC. K853655 UNK

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention