FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3830287 · Received May 23, 2014

Report

Report Number
9616091-2014-00931
Event Type
Malfunction
Date Received
May 23, 2014
Report Date
April 11, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER THE SPOKE IS BROKEN ON REAR WHEEL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
307928 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T420RDA

Patients

Seq Age Sex Outcome Treatment
1 Other