Voluntary Recall for Glucagon ® Emergency Kit for Low Blood Sugar

  • October 21, 2021

    On September 26, Eli Lilly and Company voluntarily recalled Glucagon® Emergency Kit for Low Blood Sugar.  There was a product complaint reporting that the vial of Glucagon was in liquid form instead of the powder form. The use of the liquid form of this product may fail to treat severe low blood sugar due to loss of potency.

    Members are advised to consult with their doctor to confirm if they received an affected lot, and if appropriate, about alternative treatment options.

    For details about the recalled products including product name, lot number, and expiration date, visit the Food and Drug Administration website.

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