FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 4121619 · Received September 26, 2014

Report

Report Number
1031452-2014-11163
Event Type
Malfunction
Date Received
September 26, 2014
Report Date
September 5, 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 INDEPENDENT REPAIR CENTER, THE UNIT WAS ALARMING OR RED LIGHT. THE KEY FAILURE WAS THE HEAT EXCHANGER TO THE COMPRESSOR WAS LEAKING. AN ADDITIONAL MALFUNCTION WAS THE ON/OFF SWITCH TO THE CONTROL PANEL HAD A SHORT CIRCUIT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
601954 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC10LX

Patients

Seq Age Sex Outcome Treatment
1 Other