FDA Adverse Event Malfunction Summary report: N

POWERED WHEELCHAIR

MDR report key: 3961516 · Received July 28, 2014

Report

Report Number
1525712-2014-04050
Event Type
Malfunction
Date Received
July 28, 2014
Report Date
June 19, 2014
Manufacturer
UNKNOWN
Product Code
ITI
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 MENTIONED THAT CHAIR HAD TWO JOYSTICK PROBLEMS AND A BRAKE ISSUE BUT HE DID NOT REMEMBER WHAT THE PROBLEM WAS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
438037 POWERED WHEELCHAIR 890.3860 ITI UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 Other