FDA Adverse Event Malfunction Summary report: N

POWERED WHEELCHAIR

MDR report key: 3921179 · Received July 9, 2014

Report

Report Number
3008262382-2014-00236
Event Type
Malfunction
Date Received
July 9, 2014
Report Date
June 4, 2014
Manufacturer
INVACARE REHABILITATION EQUIP
Product Code
ITI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER DEALER, RIGHT MOTOR REPLACED. CHAIR WAS VEERING TO THE RIGHT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
400343 POWERED WHEELCHAIR 890.3860 ITI INVACARE REHABILITATION EQUIP M41SRR

Patients

Seq Age Sex Outcome Treatment
1 Other