FDA Adverse Event Malfunction Summary report: N

POWERED WHEELCHAIR

MDR report key: 2914543 · Received January 14, 2013

Report

Report Number
1525712-2013-00357
Event Type
Malfunction
Date Received
January 14, 2013
Date of Event
December 17, 2012
Report Date
January 14, 2013
Manufacturer
INVACARE TAYLOR STREET
Product Code
ITI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

A DEALER REPORTED THAT A LEFT MOTOR IS WIRED WRONG. THE PROGRAMMING SHOWS A M91 CHAIR AND THIS DEVICE IS A UNSPECIFIED TDX POWERED WHEELCHAIR AND WAS NOTED PERFORMING OPPOSITE COMMANDS. A SUPPLEMENTAL REPORT WILL BE FILED IF ANY FURTHER INFORMATION IS RECEIVED. NO INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
20829 POWERED WHEELCHAIR 890.3860 ITI INVACARE TAYLOR STREET TDX

Patients

Seq Age Sex Outcome Treatment
1 Other