FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3123030 · Received May 21, 2013

Report

Report Number
9616091-2013-00852
Event Type
Malfunction
Date Received
May 21, 2013
Report Date
April 24, 2013
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

DEALER STATES ARMS FALL ALL THE WAY BACK AND SEAT IS RIPPED. PLEASE REPAIR AS NECESSARY. DEALER HAS NO ONE TO REPAIR THE CHAIR SO NEEDS TO SEND IN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
224648 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9XT

Patients

Seq Age Sex Outcome Treatment
1 Other