FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4201707 · Received October 27, 2014

Report

Report Number
9616091-2014-02247
Event Type
Malfunction
Date Received
October 27, 2014
Report Date
October 6, 2014
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

END USER ALLEGES THAT THE SPRING FELL OUT OF THE FRONT RIGGING FOOT PLATE AND WAS LOST. STATES THIS CAUSED THE PART TO COME APART AND BECOME UNUSABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
682170 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T4

Patients

Seq Age Sex Outcome Treatment
1 Other