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Anticonvulsant Recalled
02/28/2019
The recall affects bottles from lot C802676 (Exp. 3/20), which were distributed throughout the United States.
Dr. Reddy's Laboratories voluntarily initiated the recall January 31, 2019. On February 15, 2019, the FDA designated the recall Class II, communicating use of the drug may cause temporary or medically reversible adverse health consequences or a remote possibility of serious harm.
Divalproex sodium is a prescription anticonvulsant medication used to treat seizure disorders as well as bipolar disorder, and to prevent migraine headaches.
—Jolynn Tumolo
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