FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4240778 · Received November 10, 2014

Report

Report Number
9616091-2014-02419
Event Type
Malfunction
Date Received
November 10, 2014
Report Date
October 22, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KY, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

THE DEALER HAS STATED THE ARM PADS HAVE BEEN RIPPED OFF OF THE CHAIR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
721673 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T4

Patients

Seq Age Sex Outcome Treatment
1 Other