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Hyoscyamine Sulfate Recall

Date: 09/23/16

On September 16, 2016 the U.S. Food and Drug Administration (FDA) released a product recall to the wholesale and retail level, including hospitals and pharmacies. The recall involves Hyoscyamine sulfate (0.125mg) manufactured by Virtus Pharmaceuticals Opco II, LLC (Virtus). Virtus Pharmaceuticals is voluntarily recalling seven batches of Hyoscyamine sulfate (0.125mg).

Virtus Pharmaceuticals is working as quickly as possible and in collaboration with the U.S. Food and Drug Administration (FDA) to recall affected products from the marketplace, including those in the possession of patients.

Click here for more information about this recall.



Last Updated: 04/15/2020