FDA Adverse Event Malfunction Summary report: N

MECHANICAL (MANUAL) WHEELCHAIR

MDR report key: 4120176 · Received September 25, 2014

Report

Report Number
1525712-2014-06341
Event Type
Malfunction
Date Received
September 25, 2014
Report Date
July 1, 2014
Manufacturer
INVACARE TAYLOR STREET
Product Code
IOR
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER DEALER CALLED IN AND STATED THAT THE FRAME WAS BENT ON THE CHAIR. WHEN DEALER WAS ASKED WHAT CAUSED THE ISSUE, DEALER STATED THAT HE DOES NOT HAVE ENOUGH INFORMATION TO PROVIDE TO ME AT THIS TIME AND WILL CALL BACK AT A LATER DATE WHEN HE CAN SPEAK TO THE TECHNICIAN THAT REQUESTED THE QUOTE. UNABLE TO OBTAIN ANY ADDITIONAL INFORMATION AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
599191 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVACARE TAYLOR STREET RVL

Patients

Seq Age Sex Outcome Treatment
1 Other