FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 4240999 · Received November 10, 2014

Report

Report Number
3008262382-2014-01926
Event Type
Malfunction
Date Received
November 10, 2014
Report Date
October 20, 2014
Manufacturer
INVACARE REHABILITATION EQUIP
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

INDEPENDENT REPAIR CENTER: CUSTOMER ALLEGED UNIT WILL NOT START AND THE KEY FAILURE IS THE CAPACITOR IS DEFECTIVE

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
722049 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE REHABILITATION EQUIP IRC5P

Patients

Seq Age Sex Outcome Treatment
1 Other