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 |