US Drug Recall Register
Class III · Low risk Terminated Initiated Oct 5, 2021 (5 years ago)

Cetirizine hydrochloride, 10 mg tablets, 90-count bottle, Distributed by: A-S Medications…

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

Why it was recalled

Labeling: Not Elsewhere classified: Product was relabeled as 90 tablet count product although it was a manufacturer in a box with 30 tablet count tablets.

What was recalled

Cetirizine hydrochloride, 10 mg tablets, 90-count bottle, Distributed by: A-S Medications Solutions, Libertyville, IL 60048, Mfg: Major Pharmaceuticals, Livonia, MI 48152, NDC: 50090-5510-3

Recalling firm
A-S Medication Solutions LLC.
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0096-2022

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.

Other Chloride recalls

See all