FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 3946082 · Received July 21, 2014

Report

Report Number
3008262382-2014-00327
Event Type
Malfunction
Date Received
July 21, 2014
Report Date
May 29, 2014
Manufacturer
INVACARE REHABILITATION EQUIP
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TW
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

DEALER STATES THAT THE COMPRESSOR STOPPED WORKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
424683 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE REHABILITATION EQUIP IRC5P

Patients

Seq Age Sex Outcome Treatment
1 Other