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Xultophy

FDA classifies Novo Nordisk insulin pen recalls as Class I

June 11, 2021 By Brian Buntz

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In May, Novo Nordisk announced that it voluntarily recalled 1,468 product samples related to its Levemir, Tresiba, Fiasp, Novolog and Xultophy insulin lines. The products were held at sub-freezing temperatures, prompting the FDA to recently classify the recalls as Class I. FDA uses the Class I designation for situations where there is “a reasonable probability” […]

Filed Under: Auto-injectors, Diabetes, Drug-Device Combinations, Food & Drug Administration (FDA) Tagged With: FDA, Fiasp, https://www.drugdiscoverytrends.com/pharma50/novo-nordisk/, Levemir, Novo Nordisk, Novolog, recalls, Tresiba, Xultophy

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