February 28, 2001Oxygen, USP, liquid, in
Cryogenic Home Units Recalled
OH (SafetyAlerts) - The Food and
Drug Administration (FDA) said today that Kern Medical Inc. dba Dasco Home Medical
Equipment Company is recalling certain lots of its Oxygen, USP, liquid, in
Cryogenic Home Units because of an improper oxygen analyzer was used for identity testing.
This is the first public notice of
this Class III
recall issued by FDA.
Oxygen, USP, liquid, in Cryogenic Home Units.
Lot # Serial #
Kern Medical Inc. dba Dasco Home Medical Equipment Company, Alliance, OH.
Manufacturer, by telephone on 1/3/01.
Firm-initiated recall ongoing.
Questions concerning this recall may be directed
to the FDA at 1-888-INFO-FDA.
Notice of this product warning was sent via email
to SafetyAlerts subscribers February
28, 2001. For more information regarding the SafetyAlerts free email alert service
please click here.