FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 4232831 · Received November 6, 2014

Report

Report Number
1031452-2014-17860
Event Type
Malfunction
Date Received
November 6, 2014
Report Date
October 16, 2014
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER INDEPENDENT REPAIR CENTER, THE UNIT WAS ALARMING OR RED LIGHT. THE KEY FAILURE WAS THE VALVE OPERATOR TO THE 4 WAY VALVE STICKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
713955 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

Patients

Seq Age Sex Outcome Treatment
1 Other