FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 4172237 · Received October 15, 2014

Report

Report Number
1031452-2014-14052
Event Type
Malfunction
Date Received
October 15, 2014
Report Date
September 23, 2014
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER PROVIDER THE REPAIR CENTER STATEMENT ALLEGED LOW O2/ALARM WILL NOT FUNCTION AND THE KEY FAILURE IS THE BARBED FITTING IS LEAKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
653872 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5P

Patients

Seq Age Sex Outcome Treatment
1 Other