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