FDA Adverse Event Malfunction Summary report: N

PLATINUM 10 CONCENTRATOR 9153642104

MDR report key: 4813313 · Received June 2, 2015

Report

Report Number
1031452-2015-13919
Event Type
Malfunction
Date Received
June 2, 2015
Report Date
May 5, 2015
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

NO END USER INFORMATION PROVIDED. THE PRODUCT WAS EVALUATED AND REPAIRED BY AN INDEPENDENT REPAIR CENTER. A FOLLOW-UP WILL BE SENT IF ADDITIONAL INFORMATION IS RECEIVED.

Description of Event or Problem · 1

PER THE INDEPENDENT REPAIR CENTER, THE CUSTOMER ALLEGED PROBLEM IS THE ALARM WILL NOT FUNCTION. THE KEY FAILURE IS THE POWER SWITCH HAS A SHORT CIRCUIT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
355456 PLATINUM 10 CONCENTRATOR 9153642104 GENERATOR, OXYGEN, PORTABLE CAW INVACARE FLORIDA OPERATIONS IRC10LX

Patients

Seq Age Sex Outcome Treatment
1 Other