Published by Pure Edge Nutrition, LLC is recalling its widely used weight loss product, Bella Vi, following the discovery that it contains sibutramine, a medication removed from the U.S. marketplace in 2010. This drug can lead to serious side effects such as cardiac arrest, seizures, strokes, and irregular heartbeats. Individuals who have Bella Vi are advised to stop using it at once and dispose of any leftover product.
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Bella Vi Lawsuit Overview
Bella Vi lawsuits are being filed against Pure Edge Nutrition, LLC due to the presence of sibutramine, a dangerous drug ingredient that was not disclosed on product labels. The primary allegations focus on the company’s failure to inform consumers that their “all-natural” dietary supplement contained a prescription medication that was banned from the U.S. market in 2010 due to severe cardiovascular risks.
The FDA issued a recall for Bella Vi products sold between March and September 2013 after discovering the hidden drug ingredient. These lawsuits seek compensation for individuals who suffered serious health complications from using what they believed was a safe, natural weight loss supplement.
Latest Bella Vi Lawsuit Updates
- 2013 – FDA issued recall notice for all Bella VI products after discovering undisclosed sibutramine in the diet pills, warning consumers of life-threatening cardiovascular risks and drug interactions [1].
Bella Vi Injuries & Side Effects
The presence of sibutramine in Bella VI has been linked to a range of serious cardiovascular and neurological complications that can be life-threatening.
Serious side effects reported include:
- Cardiovascular complications: Heart attacks, strokes, and cardiac arrhythmias
- Blood pressure issues: Substantially increased blood pressure and elevated pulse rate
- Neurological effects: Seizures and other brain-related complications
- Drug interactions: Life-threatening interactions with other medications
Do You Qualify for a Bella Vi Lawsuit?
You may qualify for a Bella Vi lawsuit if:
- You used Bella Vi products between March and September 2013
- You experienced serious side effects including cardiovascular complications, seizures, strokes, or irregular heartbeats
- The injuries required medical treatment or hospitalization
- You can provide medical documentation linking your injuries to Bella VI use
Bella Vi Recall Information
The FDA issued a recall for Bella Vi products in 2013 after discovering they contained sibutramine, a drug ingredient not listed on the label. According to an FDA press release, the administration warns about sibutramine:
“These products pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and can present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. These products can also interact in life-threatening ways with other medications a consumer may be taking [2].”
Products affected by the Bella Vi recall include:
- Bella Vi Insane Bee Pollen Capsules
- Bella Vi BTrim Ultimate Boost
- Bella Vi BTrim Max
- Bella Vi Extreme Accelerator
- Bella Vi Insane Amp’d
- Bella Vi Amp’d Up
What is Sibutramine?
Originally sold under the brand name Meridia, sibutramine is a prescription weight loss drug that suppresses the appetite by altering brain neurotransmitters. Sibutramine was recalled in October 2010 after it was linked to severe (in some cases life-threatening) cardiovascular health complications. A study determined that patients with a history of heart disease were significantly more likely to suffer a heart attack, stroke, cardiac arrhythmia, or seizure.
Check out our website to find out which diet supplement lawsuits our lawyers are currently accepting.
Statute of Limitations for Bella Vi Lawsuits
Time limits for filing Bella Vi lawsuits vary by state, typically ranging from 1-6 years from the date of injury discovery. Given that the Bella Vi recall occurred in 2013, it is critical to act quickly as statute of limitations deadlines may be approaching. Some states have specific provisions for product liability cases involving undisclosed pharmaceutical ingredients that may extend filing deadlines.
FAQs
1. Why are Bella Vi lawsuits being filed?
Bella VI lawsuits are being filed due to severe side effects, undisclosed harmful ingredients, and lack of proper FDA approval, causing health risks.
2. What are the harmful ingredients in Bella Vi?
The harmful ingredients in Bella VI include undeclared pharmaceuticals like sibutramine, which can cause cardiovascular issues, and other unapproved substances posing health risks.
3. Who can file a Bella Vi lawsuit?
Individuals who suffered severe side effects or health complications after using Bella Vi can file a lawsuit for compensation.
4. What compensation can be sought in a Bella Vi lawsuit?
Compensation that can be sought in a Bella VI lawsuit includes medical expenses, lost wages, pain and suffering, and punitive damages for those harmed by Bella Vi supplements.
5. When was Bella Vi recalled?
Bella Vi was recalled in 2013 after the FDA discovered it contained sibutramine, a dangerous drug ingredient not listed on the product label.
6. What makes sibutramine dangerous?
Sibutramine was banned from the U.S. market in 2010 because it significantly increases blood pressure and pulse rate, leading to heart attacks, strokes, and other life-threatening cardiovascular complications.
7. How long were Bella Vi products sold?
According to the FDA, Bella Vi diet pills were sold between March and September 2013 before the recall was issued.
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References
- https://www.fda.gov/drugs/medication-health-fraud/public-notification-perfect-body-solutions-and-burn-7-contain-hidden-drug-ingredient
- https://web.archive.org/web/20160820071420/http://www.fda.gov/Safety/Recalls/ucm390693.htm