FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 3971524 · Received July 31, 2014

Report

Report Number
3008262382-2014-00438
Event Type
Malfunction
Date Received
July 31, 2014
Report Date
June 26, 2014
Manufacturer
INVACARE REHABILITATION EQUIP
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PER EMAIL - WILL RUN ABOUT 1 MIN AND THEN RED LIGHT AND SHUT DOWN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
447663 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE REHABILITATION EQUIP IRC5P

Patients

Seq Age Sex Outcome Treatment
1 Other