FDA Adverse Event
Summary report: N
CHARLOTTE CAROLINA JONES FRACTURE SYSTEM
MDR report key: 1844955
·
Received September 9, 2010
Report
- Report Number
- 1844955
- Date Received
- September 9, 2010
- Date of Event
- August 20, 2010
- Report Date
- August 31, 2010
- Manufacturer
- WRIGHT MEDICAL
- Product Code
- HWC
- Report Source
- User Facility report
- Reporter Location
- MO, US
Narratives
Description of Event or Problem · 1
CHARLOTTE CAROLINA JONES FRACTURE SYSTEM SCREW BROKE. THE PATIENT WAS IN PAIN AND UNABLE TO WORK. THE SCREW WAS SURGICALLY REMOVED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CHARLOTTE CAROLINA JONES FRACTURE SYSTEM | NON-CANNULATED SCREW | HWC | WRIGHT MEDICAL | 56015555 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 50 YR |