FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 3971044 · Received July 31, 2014

Report

Report Number
1031452-2014-04982
Event Type
Malfunction
Date Received
July 31, 2014
Report Date
June 26, 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

CUSTOMER FORWARDED A SPREADSHEET WITH MULTIPLE UNITS WITH VARIOUS ISSUES. SPECIFIC DETAILS TO THE SYMPTOM OF THE PRODUCT NOT AVAILABLE. THE ONLY NOTE WAS MADE BY THE TBM STATING THE UNITS ARE SHUTTING DOWN. SPREADSHEET ONLY DETAILS WHICH PART WAS REPLACED. ON THIS UNIT THEY STATE THEY HAVE REPLACED THE FOLLOWING COMPONENT- COMPRESSOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
448206 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

Patients

Seq Age Sex Outcome Treatment
1 Other