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July 25, 2000

JPI Jones Daniels Pharmaceuticals Levoxyl Recalled

St. Louis, MO (SafetyAlerts) - The Food and Drug Administration (FDA) today reported that Jones Pharma, Inc. is conducting a recall of JPI Jones Daniels Pharmaceuticals Levoxyl because the milligram conversion on the unit blisters is incorrectly declared as 0.75 mg.

JPI Jones Daniels Pharmaceuticals Levoxyl (Levothyroxine Sodium Tablets), 75 mcg (0.075 mg), Rx, packaged in unit-dose strips 10/10-tablet strips per box.

Recall #D-434-0.  Class III

Lot #6221 EXP 02/01.

Daniels Pharmaceuticals, St. Petersburg, Florida.

Jones Pharma, Inc., St. Louis, Missouri, by telephone on May 8, 2000. Firm-initiated recall ongoing.  This is the first public notice issued by the FDA.


440 10/10-tablet strip boxes were distributed.

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 SafeMail subscribers July 25, 2000.

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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