FDA Adverse Event Injury Summary report: N

UNKNOWN DEPUY 56X28 10DEG HIP LINER

MDR report key: 3832736 · Received May 27, 2014

Report

Report Number
1818910-2014-19455
Event Type
Injury
Date Received
May 27, 2014
Date of Event
April 30, 2014
Report Date
April 30, 2014
Manufacturer
DEPUY ORTHOPAEDICS, INC.1818910
Product Code
KWA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL NARRATIVE: 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 PATIENT WAS REVISED TO ADDRESS POLY WEAR OF THE LINER AND LOOSENING OF THE ACETABULAR SHELL. DOI: UNK DOR: (B)(6) 2014 (LEFT HIP).THE DEVICES ASSOCIATED WITH THIS REPORT WERE NOT RETURNED. REVIEW OF THE DEVICE HISTORY RECORDS AND/OR A COMPLAINT DATABASE SEARCH WAS NOT POSSIBLE AS THE PRODUCT AND LOT CODES REQUIRED WERE NOT PROVIDED. REQUESTS FOR ADDITIONAL INVESTIGATIONAL INPUTS WERE MADE IN ACCORDANCE WITH WI-7915 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. 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

THE PATIENT WAS REVISED TO ADDRESS POLY WEAR OF THE LINER AND LOOSENING OF THE ACETABULAR SHELL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
311033 UNKNOWN DEPUY 56X28 10DEG HIP LINER HIP ACETABULAR INSERT/LINER KWA DEPUY ORTHOPAEDICS, INC.1818910 UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 57 YR Required Intervention