FDA Adverse Event Injury Summary report: N

ENDURANCE SZ 2 STD OFFSET

MDR report key: 4101350 · Received September 19, 2014

Report

Report Number
1818910-2014-28468
Event Type
Injury
Date Received
September 19, 2014
Date of Event
August 20, 2014
Report Date
August 20, 2014
Manufacturer
DEPUY ORTHOPAEDICS, INC.1818910
Product Code
JDI
PMA / PMN Number
PK904351
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MN, 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

NO DEVICE ASSOCIATED WITH THIS REPORT WAS RECEIVED FOR EXAMINATION. A WORLDWIDE COMPLAINT DATABASE SEARCH FOUND NO OTHER REPORTED INCIDENTS AGAINST THE PROVIDED PRODUCT/LOT COMBINATIONS SINCE RELEASE FOR DISTRIBUTION. BASED ON PREVIOUS INVESTIGATIONS THIS COMPLICATION OF JOINT REPLACEMENT IS UNLIKELY TO HAVE BEEN THE RESULT OF A DEVICE FAILING TO MEET REQUIRED SPECIFICATIONS. THE INFORMATION RECEIVED WILL BE RETAINED FOR POTENTIAL SERIES INVESTIGATIONS IF TRIGGERED BY TREND ANALYSIS, POST MARKET SURVEILLANCE, OR OTHER EVENTS WITHIN THE QUALITY SYSTEM. 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.

Description of Event or Problem · 1

THE PATIENT WAS REVISED BECAUSE OF OSTEOLYSIS, INSTABILITY, AND LOOSENING OF THE FEMORAL STEM AT THE CEMENT/IMPLANT INTERFACE, UNKNOWN CEMENT MFG.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
582692 ENDURANCE SZ 2 STD OFFSET HIP FEMORAL STEM/SLEEVE JDI DEPUY ORTHOPAEDICS, INC.1818910 SS8AH1

Patients

Seq Age Sex Outcome Treatment
1 73 YR Required Intervention