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Meclizine Hydrochloride Tablets 12.5 mg
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DRUG RECALLMODERATE

Meclizine Hydrochloride Tablets 12.5 mg

American Health Packaging is recalling Meclizine Hydrochloride 12.5 mg tablets (NDC 60687-775-65 and 60687-775-11) due to failed tablet specifications.

What to do

Stop using this medication and contact your pharmacy or healthcare provider immediately for a replacement or alternative treatment.

Posted
Updated
Recall No.
D-0418-2026
Agency
Firm
Amerisource Health Services LLC
Recall ID
98526
Status
ONGOING

Why it was recalled

Failed tablet specifications.

How to identify it

Meclizine Hydrochloride Tablets, USP 12.5 mg, (a) 50 Tablets [5 x 10] (NDC 60687-775-65) (b) 12.5 mg Individual Dose ( NDC 60687-775-11), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio, 43217.

Where it was sold

Distributed in US.

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Editorial summary by Recall Canary · last updated 2026-04-27 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification