FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4133267 · Received October 1, 2014

Report

Report Number
9616091-2014-02060
Event Type
Malfunction
Date Received
October 1, 2014
Report Date
September 12, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE END USER STATES HER HUSBAND WAS TRANSFERRING OUT OF THE CHAIR AND THE ARM PAD ON THE LEFT HAS BROKEN OFF.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
611669 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T420RDAP

Patients

Seq Age Sex Outcome Treatment
1 Other