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More Defective Heart Tablets Recalled

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Caraco-brand Digoxin Tablets are being recalled today by A-S Medication Solutions, LLC.  The recalled tablets may differ in size, a defect which could impact both their safety and efficacy.

The Digoxin tablet recall includes all 0.25 mg tablets distributed prior to March 31, 2009, which are not expired and are within the expiration date of August, 2011.  The recalled Digoxin tablets involve those bearing NDC Number 54569-5758-0 (30-count).

Digoxin is a drug used to treat heart failure and abnormal heart rhythms. According to the Food & Drug Administration (FDA), an overdose  may pose a risk of Digoxin toxicity in patients with renal failure. Digoxin toxicity can cause nausea, vomiting, dizziness, low blood pressure, cardiac instability, and bradycardia. Death can also result from excessive Digoxin intake.

A lower than labeled dose may lack  efficacy, potentially resulting in cardiac instability.

These recalled Digoxin tablets were supplied by  Caraco Pharmaceuticals, which in March had also recalled several lots of Digoxin tablets for the same reason.

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