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2. The recall is a result of two reports outside of the U.S. of failure to activate the device due to a potential defect in a supplier component. That defect could make it difficult to activate during an emergency.
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3. “The recall impacts the 0.3 mg and 0.15 mg strengths of EpiPen Auto-Injector. None of the recalled lots include the authorized generic for EpiPen Auto-Injector, which is also manufactured by Meridian Medical Technologies,” according to a company statement.
Find out more about specific recalled products.
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