FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 3800013 · Received May 8, 2014

Report

Report Number
1031452-2014-01239
Event Type
Malfunction
Date Received
May 8, 2014
Report Date
March 31, 2014
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATED THAT THE (B)(4) CONCENTRATOR IS NOT ALARMING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
278974 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5P02V

Patients

Seq Age Sex Outcome Treatment
1 Other