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Recall of Pantoprazole Sodium for Injection 40mg/vial
Posted By Admin on February 26, 2018
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On December 4, 2017, AuroMedics Pharma LLC initiated a voluntary recall of one lot of Pantoprazole Sodium for Injection. The product was distributed nationwide to wholesalers and/or hospitals on August 7, 2017 in the United States. This recall was classified as a Class I Recall on February 8, 2018, by the Food and Drug Administration (FDA).

The product from the lot was found to contain glass particles in the vial.

Please visit https://www.fda.gov/Safety/Recalls/ucm589694.htm for more information.