FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4212448 · Received October 30, 2014

Report

Report Number
9616091-2014-02294
Event Type
Malfunction
Date Received
October 30, 2014
Report Date
October 10, 2014
Manufacturer
INVAMEX
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER IS REPORTING THAT OUT OF BOX, THAT THE BAR ON THE RIGHT SIDE OF THE SEAT FRAME IS BENT AT THE WELD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
697445 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX TREX28RP

Patients

Seq Age Sex Outcome Treatment
1 Other