FDA Adverse Event Malfunction Summary report: N

POWERED WHEELCHAIR

MDR report key: 3222891 · Received July 12, 2013

Report

Report Number
9616091-2013-01203
Event Type
Malfunction
Date Received
July 12, 2013
Report Date
June 20, 2013
Manufacturer
INVAMEX
Product Code
ITI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KS, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

CUSTOMER STATES THE CHROME HANDRIMS ARE CHIPPED AND PEELING ON THE WHEELS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
321709 POWERED WHEELCHAIR 890.3860 ITI INVAMEX T4

Patients

Seq Age Sex Outcome Treatment
1 Other