Class II · Moderate riskTerminated 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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