US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 30, 2023 (3 years ago)

Sucralfate Oral Suspension 1g per 10mL, FOR ORAL ADMINISTRATION ONLY (414 mL bottle), Rx…

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

Why it was recalled

Superpotent/Subpotent single ingredient Drug: Out of Specification Assay results

What was recalled

Sucralfate Oral Suspension 1g per 10mL, FOR ORAL ADMINISTRATION ONLY (414 mL bottle), Rx Only, Manufactured and Distributed by: VistaPharm, Inc. Largo, FL 33771, NDC 66689-305-16

Recalling firm
VistaPharm LLC
NDC code
66689-305-16
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1149-2023

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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