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Recalls & Warnings June 07, 2017 FDA Warns Seller of Probiotic and Omega-3 Supplements for Manufacturing Violations On May 22, 2017, the FDA issued a warning letter to BioTE Medical, LLC following a facility inspection which found its products, including BioTE DIM, BiotTE Probiotic, BioTE Iodine Plus, and BioTE Omega 3 to be adulterated because they were prepared, packed, or held under

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