FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3073586 · Received April 23, 2013

Report

Report Number
9616091-2013-00688
Event Type
Malfunction
Date Received
April 23, 2013
Report Date
March 28, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

THE CONSUMER REPORTED THAT THE CASTER BECAME STUCK IN A DOOR AND THE PLASTIC SPOKES CRACKED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
173575 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX GVTRSX58

Patients

Seq Age Sex Outcome Treatment
1 Other