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SafetyAlerts
February 28, 2001

Oxygen, USP, liquid, in Cryogenic Home Units Recalled

Alliance, 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.

PRODUCT
Oxygen, USP, liquid, in Cryogenic Home Units.

Recall #D-077-1.

CODE:
Lot # Serial #
120400-7 C065A86
120400-6 S021185
120400-7 C034K08
120400-6 S027185

MANUFACTURER:
Kern Medical Inc. dba Dasco Home Medical Equipment Company, Alliance, OH.

RECALLED BY:

Manufacturer, by telephone on 1/3/01. Firm-initiated recall ongoing.

DISTRIBUTION:
Ohio.

QUANTITY:
Four.

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.

 
Selected Recent Recalls


Health Professional:

Did you know?
During 2000 there were over
1050 products recalled in the United
States for safety reasons!

How many did you hear about?

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The information contained herein has been obtained from sources that the Company believes to be reliable, however, the Company has not independently verified or confirmed the information and the recipient acknowledges that no representations or warranties are being made in connection with the use of the information.