FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 3944585 · Received July 18, 2014

Report

Report Number
1031452-2014-03851
Event Type
Malfunction
Date Received
July 18, 2014
Report Date
May 28, 2014
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

ALARMING PER REPAIR DOCUMENT. POPPET VALVE IS NOT SHIFTING PER DEALER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
422378 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

Patients

Seq Age Sex Outcome Treatment
1 Other