US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 7, 2022 (5 years ago)

Clobazam Oral Suspension 2.5 mg/mL, 120 mL bottles, Rx only, Manufactured by…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed Stability Specifications

What was recalled

Clobazam Oral Suspension 2.5 mg/mL, 120 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771, NDC 66689-058-04

Recalling firm
VistaPharm, Inc.
NDC code
66689-058-04
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0376-2022

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.

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