FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 3223537 · Received July 12, 2013

Report

Report Number
1031452-2013-01359
Event Type
Malfunction
Date Received
July 12, 2013
Date of Event
June 21, 2013
Report Date
June 21, 2013
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

THE DEALER IS REPORTING THAT THE UNIT IS NOT ALARMING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
323422 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

Patients

Seq Age Sex Outcome Treatment
1 Other