Recalls

Bacai Inc. Issues Voluntary Worldwide Recall of LiteFit USA

Silver Spring, Maryland–(ENEWSPF)–April 30, 2014.  Bacai is voluntarily recalling 13165 lot (lot number is found next to the expiration date) of LiteFit USA, to the retail and consumer level. This product is used as an herbal diet supplement and is packaged in plastic bottles of 30 softgels. Sample analysis by the FDA has revealed that this product contained sibutramine.

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Risk Statement: Sibutramine is a controlled substance that was removed from the market in October 2010…

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