FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 4093792 · Received September 16, 2014

Report

Report Number
1031452-2014-09501
Event Type
Malfunction
Date Received
September 16, 2014
Report Date
August 18, 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 STATEMENT THE UNIT WILL NOT START. THE KEY FAILURE WAS THE COMPRESSOR WAS NOISY. ADDITIONAL MALFUNCTIONS INCLUDE THE INLET FILTER WAS DIRTY, THE POWER SWITCH FOR THE CONTROL PANEL SHORT CIRCUITED, AND THE HOSE CLAMP FOR THE COMPRESSOR WAS REPLACED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
572833 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

Patients

Seq Age Sex Outcome Treatment
1 Other