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Vertigo Tablets Recalled in Two States
02/26/2021
The recall affects the following products:
- meclizine hydrochloride tablets, 12.5 mg, 100-tablet bottles (NDC 52536-129-01), from lot 18030318 (Exp. 3/21); and
- meclizine hydrochloride tablets, 25 mg, 100-tablet bottles (NDC 52536-133-01), from lots 18030329, 18030330, and 18030331 (Exp. 3/21).
Wilshire Pharmaceuticals initiated the recall February 4, 2021. The FDA designated the recall Class II on February 16, 2021. Drugs affected by Class II recalls may cause temporary or medically reversible adverse health consequences if used. While remote, a possibility of serious harm also exists.
Meclizine is a prescription antihistamine used to treat symptoms of vertigo.
—Jolynn Tumolo