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SafetyAlerts
December 6, 2000

Altana Inc. Recalls Desoximetasone Ointment

Melville, NY (SafetyAlerts) - The Food and Drug Administration (FDA) said today that Altana Inc. is recalling certain Desoximetasone Ointment because of degradation failure at 12-month stability testing.

This is the first public notice of this Class III recall issued by FDA.

PRODUCT
Desoximetasone Ointment, USP, 0.25%, in 15 and 60-gram tubes, Rx topical corticosteroid ointment, NDC #0168-0151-15 (15g) and NDC #0168-0151-60
(60g).

Recall #D-048-1.

CODE
Lot #D756 EXP 11/00.

MANUFACTURER
Altanta, Inc., Hicksville, New York.

RECALLED BY
Altana, Inc., Melville, New York, by letter dated October 6, 2000. Firm-initiated recall ongoing.

DISTRIBUTION
Nationwide.

QUANTITY
2,130 15-gram and 2,135 60-gram tubes were distributed; firm estimated that little or no product remained on market at time of recall initiation.

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 December 6, 2000.  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.