Pure Edge Nutrition recalls Bella Vi INSANE AMP'D Dietary Supplement capsules due to undeclared sibutramine and phenolphthalein, which may pose health risks. Consumers should check product details and follow official guidance.
Marketed without an Approved NDA/ANDA; product was found to contain undeclared sibutramine & phenolphthalein
Pure Edge Nutrition is recalling Bella Vi INSANE AMP'D Dietary Supplement capsules because they contain undeclared sibutramine and phenolphthalein. These substances are not approved for use in dietary supplements and could cause health risks.
The product contains undeclared sibutramine, a weight-loss drug banned in the U.S., and phenolphthalein, a laxative that can cause kidney damage. Both substances are not approved for use in dietary supplements and could lead to serious health issues.
People who purchased Bella Vi INSANE AMP'D Dietary Supplement capsules from www.BellaViProducts.com or distributors like Pure Edge Nutrition. Those with pre-existing health conditions may be at higher risk.
Check for Bella Vi INSANE AMP'D Dietary Supplement capsules, 60-count bottles sold online at www.BellaViProducts.com or distributed by Pure Edge Nutrition. The lot number is VINA2013 with an expiration date of June 12, 2015.
Look for the product name, lot number VINA2013, and expiration date June 12, 2015 on the bottle.
The product contains undeclared sibutramine and phenolphthalein, which are not approved for use in dietary supplements and could pose health risks. It is not safe to use.
Check for Bella Vi INSANE AMP'D Dietary Supplement capsules, 60-count bottles with lot number VINA2013 and expiration date June 12, 2015.
The recall record does not specify a remedy, so contact Pure Edge Nutrition for guidance.
We’ve drafted a message you can send Bella Vi to request your refund or repair — edit it as you like.
Subject: Recall D-1369-2014 — Bella Vi Bella Vi Hello, I own a Bella Vi that is covered by recall D-1369-2014 from Bella Vi. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
