FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 4180497 · Received October 17, 2014

Report

Report Number
1031452-2014-14719
Event Type
Malfunction
Date Received
October 17, 2014
Report Date
September 29, 2014
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER INDEPENDENT REPAIR CENTER, THE UNIT WOULD NOT START. THE KEY FAILURE WAS MANIFOLD VALVE STICKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
663256 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

Patients

Seq Age Sex Outcome Treatment
1 Other