FDA Adverse Event Malfunction Summary report: N

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

MDR report key: 3970831 · Received July 31, 2014

Report

Report Number
1031452-2014-04953
Event Type
Malfunction
Date Received
July 31, 2014
Report Date
June 25, 2014
Manufacturer
INVACARE FLORIDA OPERATIONS
Product Code
CAW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

PER REPAIR STATEMENT ATTACHED UNIT HAS LOW O2 AND SHOWING YELLOW LIGHT.

Description of Event or Problem · 1

PER PROVIDER, SIEVE BEDS HAVE A CAP THAT IS CRACKED. PER REPAIR STATEMENT ATTACHED UNIT HAS LOW O2 AND SHOWING YELLOW LIGHT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
448424 PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) 868.5440 CAW INVACARE FLORIDA OPERATIONS IRC5PO2V

Patients

Seq Age Sex Outcome Treatment
1 Other