Sucralfate Oral Suspension 1g per 10mL, FOR ORAL ADMINISTRATION ONLY (414 mL bottle) recall — FDA D-1149-2023
Superpotent/Subpotent single ingredient Drug: Out of Specification Assay results
Overview of recall records associated with VistaPharm LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Superpotent/Subpotent single ingredient Drug: Out of Specification Assay results
This page summarizes recall records in which the official source identifies VistaPharm LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.