FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 4220236 · Received November 3, 2014

Report

Report Number
1031452-2014-17180
Event Type
Malfunction
Date Received
November 3, 2014
Report Date
October 13, 2014
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
ND, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER GETTING TWO RED AND ONE GREEN LIGHT THEN ONE RED TWO GREEN LIGHTS AND UNIT SHUTS DOWNTHIS RECORD HAS BEEN IDENTIFIED AS PART OF CAPA (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
701941 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

Patients

Seq Age Sex Outcome Treatment
1 Other