FDA Adverse Event Injury Summary report: N

SOL SYS 1.5X12.0 CALCAR 12/14

MDR report key: 2991671 · Received March 6, 2013

Report

Report Number
1818910-2013-13276
Event Type
Injury
Date Received
March 6, 2013
Date of Event
February 22, 2013
Report Date
February 22, 2013
Manufacturer
DEPUY ORTHOPAEDICS, INC. 1818910
Product Code
LPH
PMA / PMN Number
PK953703
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE DEVICES ASSOCIATED WITH THIS REPORT WERE NOT RETURNED. A COMPLAINT DATABASE SEARCH FINDS NO OTHER REPORTED INCIDENTS AGAINST THE PROVIDED PRODUCT AND LOT COMBINATION SINCE ITS RELEASE FOR DISTRIBUTION. REVIEW OF THE DEVICE HISTORY RECORDS AND/OR A COMPLAINT DATABASE SEARCH WAS NOT POSSIBLE FOR THE ACETABULAR LINER AS THE PRODUCT AND LOT CODE REQUIRED WAS NOT PROVIDED. REQUESTS FOR ADDITIONAL INVESTIGATIONAL INPUTS WERE MADE IN ACCORDANCE WITH WI-7915 APPENDIX A; REV. D. NO ADDITIONAL INFORMATION WAS OBTAINED. THE INVESTIGATION COULD NOT DRAW ANY CONCLUSIONS REGARDING THE REPORTED EVENT WITH THE INFORMATION AVAILABLE. BASED ON THE INABILITY TO IDENTIFY A ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION WAS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT OR ADDITIONAL INFORMATION BE RECEIVED TO CHANGE THE OUTCOME OF THE PERFORMED INVESTIGATION, THE COMPLAINT WILL BE RE-OPENED.

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.

Description of Event or Problem · 1

PATIENT WAS REVISED TO ADDRESS A BROKEN, LOOSE STEM, SEVERE OSTEOLYSIS, AND PAIN. POLY WEAR WAS ALSO REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
95015 SOL SYS 1.5X12.0 CALCAR 12/14 FEMORAL HIP STEM LPH DEPUY ORTHOPAEDICS, INC. 1818910 R4TA81

Patients

Seq Age Sex Outcome Treatment
1 89 YR Required Intervention