VistaPharm NYSTATIN ORAL SUSPENSION, USP 100,000 units per mL Contains: Alcohol 0.5% v/v recall — FDA D-0019-2021
Failed Impurties/Degradation Specifications: out of specification results for an impurity for one lot
Overview of recall records associated with VistaPharm, Inc., including dates, categories and classifications where available.
Classification mix: Class III: 1.
Failed Impurties/Degradation Specifications: out of specification results for an impurity for one lot
This page summarizes recall records in which the official source identifies VistaPharm, Inc. 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.