FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3253190 · Received July 29, 2013

Report

Report Number
9616091-2013-01355
Event Type
Malfunction
Date Received
July 29, 2013
Report Date
July 12, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE DEALER IS REPORTING THAT THE REAR SPOKES ARE BROKEN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
352688 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T422RDA

Patients

Seq Age Sex Outcome Treatment
1 Other