FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 3160571 · Received June 10, 2013

Report

Report Number
9616091-2013-00968
Event Type
Malfunction
Date Received
June 10, 2013
Report Date
May 13, 2013
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED THAT THE 9XT MANUAL WHEELCHAIR HAS WOBBLY BACK CANES, BROKEN ARMS AND SIDE FRAME IS WORN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
259982 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX 9XT

Patients

Seq Age Sex Outcome Treatment
1 Other