JAMP Pharma Corporation is recalling its digoxin tablets because some bottles may contain an incorrect dose, Health Canada announced in an advisory. The drug-maker said its 0.0625 and 0.125 mg digoxin ...

What to do: Return your JAMP Digoxin 0.0625 mg tablets to your pharmacy for replacement as soon as possible. Until you can return them, continue to take your JAMP Digoxin, but do not take any tablets ...

The Food and Drug Administration announced the recall of one lot of Digoxin Tablets USP, 0.125 mg, and one lot of Digoxin Tablets USP, 0.25 mg. Bottles of Digoxin Tablets, USP 0.125 mg are incorrectly ...

AS Medication Solutions, a drug repackage company, announced today that all Caraco brand digoxin 0.25mg tablets, distributed prior to March 31, 2009, which are not expired and are within the ...

Caraco Pharmaceutical Laboratories is recalling all lots of Digoxin tablets because the product might vary in size and deliver different doses of the drug. Spokesman Thomas Versosky said there have ...

Caraco Pharmaceutical has issued a nationwide voluntary recall to the consumer level of all Caraco brand digoxin 0.125mg and 0.25mg tablets distributed prior to March 31, 2009, which are not expired ...

WOODCLIFF LAKE, N.J. — Par Pharmaceutical on Thursday announced that it has entered into an exclusive U.S. supply and distribution agreement with Covis Pharma S.a.r.l. to distribute the authorized ...

WASHINGTON, March 31 (UPI) -- The U.S. Food and Drug Administration announced the recall of Caraco-brand digoxin tablets with an expiration date of September 2011 due to a safety hazard. The FDA said ...

April 29, 2008 (Morristown, NJ) -The manufacturer of Digitek digoxin tablets is recalling the product, saying that it may have accidentally released pills that are double the normal thickness, ...

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Digoxin recalled over mislabeling Two lots of Digoxin were mislabeled, leading to a recall. Digoxin is used for the treatment of mild to moderate heart failure in children and adults. By Debbie Lord, ...