FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 3953342 · Received July 23, 2014

Report

Report Number
1031452-2014-04242
Event Type
Malfunction
Date Received
July 23, 2014
Report Date
June 5, 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

CLAIMANT ALLEGED CONCENTRATOR 4 WAY VALVE NOT SHIFTING. REPAIR STATEMENT INDICATES UNIT WAS ALARMING AND SHUTTING DOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
431148 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2

Patients

Seq Age Sex Outcome Treatment
1 Other