Meclizine Hydrochloride Tablets
Failed tablet specifications.
Yes — there is an active recall. 2 ongoing FDA recalls mention Meclizine (16 total). Check the affected lots below.
Most common reason: Impurity / degradation (5 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Meclizine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Failed tablet specifications.
cGMP deviations: Temperature abuse
Labeling: Label mix-up: Incorrect label placed on product. Shipper cases labeled Meclizine Hydrochloride Tablets contain bottles incorrectly labeled as PredniSONE Tablets. The tablets in the bottles are Meclizine Hydrochloride
Labeling: Incorrect Instructions
Failed Dissolution Specifications
Failed Dissolution Specifications
Subpotent Drug
Subpotent Drug
Subpotent Drug
Subpotent Drug
Marketed without an approved NDA/ANDA: Bottles were released prior to final approval.
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Failed Impurities/Degradation Specifications: Out of specification for impurities.
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