FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3781655 · Received April 30, 2014

Report

Report Number
9616091-2014-00784
Event Type
Malfunction
Date Received
April 30, 2014
Report Date
March 26, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER DEALER THE COMPOSITE FOOTPLATE IS CRACKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
260027 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9XT

Patients

Seq Age Sex Outcome Treatment
1 Other