FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 4211386 · Received October 29, 2014

Report

Report Number
1031452-2014-16593
Event Type
Malfunction
Date Received
October 29, 2014
Report Date
October 8, 2014
Manufacturer
INVACARE REHABILITATION EQUIP
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER REPORTS THE UNIT IS ALARMING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
693847 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE REHABILITATION EQUIP IRC5PO2V

Patients

Seq Age Sex Outcome Treatment
1 Other