FDA Adverse Event Malfunction Summary report: N

TRIDENT

MDR report key: 2071866 · Received April 21, 2011

Report

Report Number
MW5020398
Event Type
Malfunction
Date Received
April 21, 2011
Date of Event
February 23, 2006
Report Date
April 21, 2011
Product Code
MEH
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
OR, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

"H", 20 MINUTES AND MAKES RIDING IN A CAR DIFFICULT. NOW I EVEN HAVE PAIN LYING DOWN AND IT IS AFFECTING MY WORK AND LIFE. I AM ON CONSTANT PAIN MEDS THAT ONLY MASK THE PROBLEM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TRIDENT TRIDENT HEMISPHERICAL ACETABULAR SHELL MEH 11165301

Patients

Seq Age Sex Outcome Treatment
1 53 YR Other