US Drug Recall Register
Class III · Low risk Terminated Initiated Oct 1, 2019 (7 years ago)

Zentrip (meclizine Hydrochloride), 25 mg strips, 8-strips per box, Distributed by Sato…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Subpotent Drug

What was recalled

Zentrip (meclizine Hydrochloride), 25 mg strips, 8-strips per box, Distributed by Sato Pharmaceutical INC. 20695 S. Western Ave., Suite 240 Torrence, CA 90501, NDC 49873-803-01. UPC 4987301603

Recalling firm
Sato Pharmaceutical Inc.
NDC code
49873-803-01
Origin
CA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0322-2020

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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