FDA Adverse Event Injury Summary report: N

PINNACLE SECTOR II CUP 52MM

MDR report key: 3932674 · Received July 14, 2014

Report

Report Number
1818910-2014-23281
Event Type
Injury
Date Received
July 14, 2014
Date of Event
June 20, 2014
Manufacturer
DEPUY ORTHOPAEDICS, INC.
Product Code
KWA
PMA / PMN Number
PK073504
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IN, 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

LINER DISLOCATED FROM THE CUP. DOI: (B)(6) 2006, DOR: (B)(6) 2014, (RIGHT HIP). THE DEVICES ASSOCIATED WITH THIS REPORT WERE NOT RETURNED. A COMPLAINT DATABASE SEARCH FINDS NO OTHER REPORTED INCIDENTS AGAINST THE KNOWN PRODUCT/LOT COMBINATION(S) SINCE RELEASE FOR DISTRIBUTION. A DHR REVIEW OR LOT SPECIFIC DATABASE SEARCH WAS NOT POSSIBLE FOR THE ADDITIONAL PRODUCT ASSOCIATED WITH THIS REPORT AS LOT CODE(S) WAS NOT PROVIDED. FOLLOW-UP FOR ADDITIONAL EVENT INFORMATION WAS CONDUCTED UTILIZING WORK INSTRUCTION WI-7915 APPENDIX A. NO ADDITIONAL INFORMATION WAS OBTAINED. THE INVESTIGATION COULD NOT DRAW ANY CONCLUSIONS REGARDING THE REPORTED EVENT. BASED ON THE INABILITY TO DETERMINE A 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

LINER DISLOCATED FROM THE CUP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
409074 PINNACLE SECTOR II CUP 52MM HIP ACETABULAR CUP KWA DEPUY ORTHOPAEDICS, INC. AA5FS1

Patients

Seq Age Sex Outcome Treatment
1 76 YR Required Intervention