FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3963921 · Received July 29, 2014

Report

Report Number
9616091-2014-01329
Event Type
Malfunction
Date Received
July 29, 2014
Report Date
June 23, 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

IT WAS REPORTED THAT THE UNIT'S RIGHT SIDE RIGGING WILL NOT STAY ON THE CHAIR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
441308 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 4V08FFR

Patients

Seq Age Sex Outcome Treatment
1 Other