FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 3903340 · Received June 30, 2014

Report

Report Number
1031452-2014-02756
Event Type
Malfunction
Date Received
June 30, 2014
Report Date
June 2, 2014
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KS, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE XPO100 CONCENTRATOR IS GETTING A 3 & 4 ERROR CODE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
379135 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS XPO100

Patients

Seq Age Sex Outcome Treatment
1 Other