FDA Adverse Event Malfunction Summary report: N

POWERED WHEELCHAIR

MDR report key: 3011876 · Received March 19, 2013

Report

Report Number
1525712-2013-02088
Event Type
Malfunction
Date Received
March 19, 2013
Report Date
February 20, 2013
Manufacturer
UNKNOWN
Product Code
ITI
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

(B)(6) -THE DEALER REPORTED THAT THE UNSPECIFIED POWER WHEELCHAIR HAD A JOYSTICK LOGGING ON WITHOUT COMMAND. THERE WAS NO INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
114498 POWERED WHEELCHAIR 890.3860 ITI UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other