FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3840922 · Received May 30, 2014

Report

Report Number
9616091-2014-00967
Event Type
Malfunction
Date Received
May 30, 2014
Report Date
April 17, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

THE ARMS ON THE CHAIR ARE LOSE WHERE THE ARMS ATTACH TO THE FRAME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
318573 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX SOLARA3G

Patients

Seq Age Sex Outcome Treatment
1 27 Other