FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 4100598 · Received September 19, 2014

Report

Report Number
1031452-2014-10021
Event Type
Malfunction
Date Received
September 19, 2014
Report Date
August 28, 2014
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Description of Event or Problem · 1

REPAIR STATEMENT CUSTOMER STATED PROBLEM: ALARM WILL NOT FUNCTION. VERIFIED: YES. KEY: POWER SWITCH SHORT CIRCUIT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
582372 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2

Patients

Seq Age Sex Outcome Treatment
1 Other