FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 2923573 · Received January 22, 2013

Report

Report Number
3004493922-2013-00157
Event Type
Malfunction
Date Received
January 22, 2013
Report Date
January 19, 2013
Manufacturer
INVACARE SUZHOU
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

(B)(4) HAS BEEN INITIATED FOR THIS ISSUE. THE MALFUNCTION HAS NOT BEEN CONFIRMED.

Description of Event or Problem · 1

(B)(4). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. PER DEALER AFTER RUNNING A FEW MINUTES THE UNIT SHUTS OFF BY ITSELF. MDR FILED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
29174 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE SUZHOU IRC5LX

Patients

Seq Age Sex Outcome Treatment
1 Other