FDA Adverse Event Injury Summary report: N

ARTICUL/EZE BALL 28 +1.5 GR

MDR report key: 3925014 · Received July 10, 2014

Report

Report Number
1818910-2014-23082
Event Type
Injury
Date Received
July 10, 2014
Date of Event
June 11, 2014
Report Date
June 11, 2014
Manufacturer
DEPUY INTERNATIONAL LTD. 8010379
Product Code
JDI
PMA / PMN Number
PK883460
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

PATIENT DISLOCATING HIP, SURGEON EXTRACTED POLY, REVISING WITH +4 10 DEGREE 32 ALTRX. DOI: UNK, DOR: (B)(6) 2014 (RIGHT HIP). 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. 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 AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY.

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.

Description of Event or Problem · 1

PATIENT DISLOCATING HIP, SURGEON EXTRACTED POLY, REVISING WITH +4 10 DEGREE 32 ALTRX.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
404675 ARTICUL/EZE BALL 28 +1.5 GR HIP FEMORAL HEAD JDI DEPUY INTERNATIONAL LTD. 8010379 UNK

Patients

Seq Age Sex Outcome Treatment
1 74 YR Required Intervention