FDA Adverse Event Injury Summary report: N

22.225ID POLY N LINER 48MM OD

MDR report key: 3964423 · Received July 29, 2014

Report

Report Number
1818910-2014-24344
Event Type
Injury
Date Received
July 29, 2014
Date of Event
July 8, 2014
Report Date
July 8, 2014
Manufacturer
DEPUY ORTHOPAEDICS, INC.
Product Code
HRY
PMA / PMN Number
PK944538
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IA, 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 DEVICE ASSOCIATED WITH THIS REPORT WAS NOT RETURNED. IT IS KNOWN THAT THE REPORTED PRODUCT IS NOW OBSOLETE. 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 WITHOUT DEVICE EXAMINATION. HOWEVER ALTHOUGH NOT RETURNED, IT WOULD NOT BE UNREASONABLE TO FIND POLY MATERIAL WEAR AFTER THE LENGTH OF TIME REPORTED AS IMPLANTED. 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 BECAUSE OF POLY WEAR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
441656 22.225ID POLY N LINER 48MM OD HIP ACETABULAR INSERT/LINER HRY DEPUY ORTHOPAEDICS, INC. 766830023

Patients

Seq Age Sex Outcome Treatment
1 58 YR Required Intervention