FDA Adverse Event Malfunction Summary report: N

POWERED WHEELCHAIR

MDR report key: 3903163 · Received June 30, 2014

Report

Report Number
1525712-2014-03282
Event Type
Malfunction
Date Received
June 30, 2014
Date of Event
May 29, 2014
Report Date
May 29, 2014
Manufacturer
INVACARE TAYLOR STREET
Product Code
ITI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
KS, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER DEALER STATED THE END USER CAME IN WITH THE ARM OF HIS CHAIR AND STATED THE TUBE THAT ATTACHES TO THE SIDE PANEL BROKE ON THE RIGHT SIDE. DEALER STATED THERE WERE NO INJURIES PERTAINING TO THE INCIDENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
380016 POWERED WHEELCHAIR 890.3860 ITI INVACARE TAYLOR STREET 3GTQSP

Patients

Seq Age Sex Outcome Treatment
1 Other