FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 4173398 · Received October 15, 2014

Report

Report Number
1031452-2014-13943
Event Type
Malfunction
Date Received
October 15, 2014
Report Date
September 23, 2014
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER INDEPENDENT REPAIR CENTER STATEMENT ALLEGED THE CAPACITOR SHORT CIRCUIT, THE UNIT IS ALARMING A RED LIGHT DUE TO THE VALVE BEING STUCK AND ZIP TIE, HEAT EXCHANGER ARE LEAKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
653028 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2

Patients

Seq Age Sex Outcome Treatment
1 Other