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The voluntary recall consists of select vitafusion products after the Company identified the possible presence of a metallic mesh material in product lots manufactured in a four-day period between October 29 and November 3, 2020. The Company is not aware of any reports of consumer illness or injury. We are taking every necessary action to recover any products that could have been impacted. We are coordinating closely with the U.S. Food & Drug Administration (FDA) and following all relevant protocols.