FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 3163504 · Received June 11, 2013

Report

Report Number
1031452-2013-01099
Event Type
Malfunction
Date Received
June 11, 2013
Date of Event
May 14, 2013
Report Date
May 14, 2013
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

PROVIDER ALLEGED 02 SENSOR IS NOT WORKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
263863 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

Patients

Seq Age Sex Outcome Treatment
1 Other