FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 4103031 · Received September 19, 2014

Report

Report Number
1031452-2014-10112
Event Type
Malfunction
Date Received
September 19, 2014
Report Date
August 28, 2014
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER REPAIR CENTER: THE UNIT WAS ALARMING/RED LIGHT AND THE KEY FAILURE WAS A VALVE WAS STUCK.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
582569 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2

Patients

Seq Age Sex Outcome Treatment
1 Other