FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 4180432 · Received October 17, 2014

Report

Report Number
1031452-2014-14709
Event Type
Malfunction
Date Received
October 17, 2014
Report Date
September 29, 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, THE UNIT'S ALARM WAS NOT FUNCTIONAL. THE KEY FAILURE WAS PE VALVE LEAKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
663097 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC10LXO2

Patients

Seq Age Sex Outcome Treatment
1 Other