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Food and Drug Administration FDA and Pure Edge Nutrition announced a voluntary recall dier Bella Vi in October Laboratory analysis from the FDA found dita hidden drug ingredient that was not listed on the label. These products can also interact in life-threatening ways with other medications a consumer may be taking.
It was withdrawn from the market on October 8,due to the risk of serious cardiovascular events. A study found that patients with pre-existing cardiovascular disease on long-term treatment were significantly more likely to have a heart attack, stroke, arrhythmia, or seizure. The Schmidt Firm, PLLC is currently accepting Bella Vi injury cases in all 50 states.
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