Safety Alerts & Recalls

What does this mean?

This recall for Dipyridamole 25 mg tablets was issued at a warehouse/pharmacy level only. The FDA and the manufacturer have determined that product already dispensed to patients does not pose a significant health risk. If you take Dipyridamole 25 mg tablets and are concerned, you should consult with your physician.

Lannett Co., Inc Recalls Select Lots of Dipyridamole 25 mg Tablets

Lannett Co., Inc is recalling four lots of Dipyridamole 25 mg tablets. Lot numbers 2008261067, 2008522883, 2008261068, and 2008522884 are being recalled because samples from these lots failed tests that measured their ability to dissolve.

Dipyridamole is used along with other drugs to reduce the risk of blood clots after heart valve replacement surgery. Dipyridamole is also sold under the brand name Persantine. This recall alert only applies these four lots of Dipyridamole 25 mg made by Lannett Co., Inc. No other dipyridamole products are involved in this recall.

To view the FDA notice about this recall, please visit: more information here

Source: FDA
Publication Date: 2010-04-02
Last Updated: 2010-04-02

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