FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3150868 · Received June 6, 2013

Report

Report Number
9616091-2013-00956
Event Type
Malfunction
Date Received
June 6, 2013
Report Date
May 9, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED THAT THE CHROME ON THE HANDRIMS OF A T4X24RDA MANUAL WHEELCHAIR IS WEARING OFF CAUSING THE USER TO CUT HER HANDS. NO MEDICAL INTERVENTION ALLEGED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
251139 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T4X24RDA

Patients

Seq Age Sex Outcome Treatment
1 Other