September 28, 2021

Search Results for: sibutramine

La Bri’s Body Health Supplements Recalled for Sibutramine

EZ Weight Loss TX is recalling all lots of La Bri's Body Health Atwomic and Xplode capsules because they contain sibutramine. That compound was banned from the U.S. in October 2010 beaus it increases blood pressure and/or pulse rate in some people. It can also interact in life-threatening ways with other medications. No adverse events have been reported to date. These products are marketed as dietary supplements. Atomic is packaged in 60- count bottles and Xplode is packaged in 30-count bottles. All lots and codes of Atomic and Xplode are included in this recall and were sold throughout the U.S. through internet sales starting in 2015. The company is asking customers to contact them to arrange for a return or refund. Stop using this product immediately. If you have experienced any … [Read more...]

Ultimate Herbal Slimcaps Recalled for Undeclared Sibutramine

Fit Firm and Fabulous is voluntarily recalling some lots of Ultimate Herbal Slimcap capsules because it contains sibutramine, a drug that was removed from the market 5 years ago. Because it contains this ingredient, the product is an unapproved drug. Sibutramine poses a threat to consumers because it substantially increases blood pressure and pulse rate in some patients and can present a significant risk for patients who have a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. This product may also interact in life threatening ways with other medications a patient is taking. No reports of illness or adverse reactions have been received to date. The product is a dietary supplement marked for weight loss called Ultimate Herbal Slimcap. It is packaged … [Read more...]

Burn 7 Capsules Recalled for Undeclared Sibutramine

Deseo Rebajar, Inc. is recalling Burn 7 Capsules, a dietary supplement to promote weight loss, because it contains undeclared Sibutramine. That is a previously controlled substance that was removed from the U.S. market in October 2010 for safety reasons. The drug substantially increases blood pressure and/or pulse rate in some people. It may present a significant risk to patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. The recalled product is Burn 7 capsules with lot #MFD: 07.18.2013 (Exp: 07.17.2015). The product was sold directly to customers from the company offices in Fajardo, Caguas and Bayamon, and through the company's website. If you purchased this product, do not use it. Return it to the place of purchase for a refund. If … [Read more...]

Maxiloss Weight Advanced Softgels Recalled for Sibutramine

Olaax Corp. is recalling the company's dietary supplement sold under the brand name Maxiloss Weight Advanced Softgels because they contain undeclared Sibutramine. FDA testing found the drug in the supplement. Sibutramine was a previously approved controlled substance that was removed from the market in October 2010 because it can substantially increase blood pressure and/or pulse rate in some patients. This may be a significant health risk to anyone with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. No illnesses or injuries have been reported to date. The recall includes all lot numbers and known to be counterfeit lot numbers of authentic lots. Any packaging types different from those listed are counterfeit. Any lot numbers not listed are … [Read more...]

Imperia Elita Vitaccino Coffee Recalled For Undeclared Drugs

Dash Exclusive is voluntarily recalling all lots of Imperia Elita Vitaccino Coffee because it contains sibutramine and fluoxetine, two drugs that are not declared on the label. This product is a weight loss and anxiety dietary supplement. FDA analysis found the presence of these compounds in the product. The company has not received any reports of adverse reactions related to the use of this recalled product. Sibutramine was an FDA-approved drug that was used as an appetite suppressant. It was withdrawn from the marketplace because of safety issues, including stroke, heart failure, and serious health risks, especially for people who have underlying heart disease. Sibutramine can significantly increase blood pressure and pulse rate. Fluxoetine is an FDA-aprpved drug that is used … [Read more...]

FDA Says Some Weight Loss, Other Supplements May Be Dangerous

The FDA has released a consumer update stating that weight loss products and other supplements, including male enhancement products, that are sold online or in stores may be dangerous because they may be illegal. Some of these dietary supplements can be made with potentially dangerous ingredients that are not listed on the label. Over the past 10 years, the FDA has waned consumers that some products that are sold over the counter contain active hidden ingredients. This is especially the case for products that are marketed for weight loss, pain relief, body building, sleep aids, and male enhancement. Some of these products are actually drugs and are falsely represented as being dietary supplements. FDA has also found products that are marketed as supplements that claim to treat or … [Read more...]

Zero Xtreme Dietary Supplement Recalled for Sibrutramine

Fat Burners Zone is recalling one lot of Zero Xtreme capsules, a dietary supplement intended for weight loss, because it is contaminated with sibutramine, according to FDA analysis. Sibutramine is an appetite suppressant that was withdrawn from the U.S. market for safety concerns. That means Zero Xtreme is an unapproved drug. Sibutramine is the active ingredient in Meridia, a drug that was marketed in the 1990s for prescription treatment of obesity. It was withdrawing 2010 after clinical dates indicated "Sibutramine poses an increased risk of heart attack and stroke." The product can substantially increase blood pressure and pulse rate, and can present a health risk for anyone with a history of coronary artery daisies, congestive heart failure, arrhythmias, and stroke. No adverse events … [Read more...]

Consent Decree Issued Against MyNicNaxs, Maker of Dietary Supplements

A federal court ordered a Florida-based company called MyNicNaxs to stop selling drugs and dietary supplements until it complies with the Federal Food, Drug, and Cosmetic Act and other requirements. The U.S. District Court for the Middle District of Florida has entered a consent decree of permanent injunction against MyNicNaxs of Deltona Florida. The company distributed weight loss and sexual enhancement products, marketed as dietary supplements, directly to consumers online through their websites. Some of these products tested positive for undeclared active pharmaceutical ingredients. Donald D. Ashley, director of the Office of Compliance in the FDA’s Center for Drug Evaluation and Research said in a statement, "Marketing products with undeclared active pharmaceutical … [Read more...]

LaBrit’s Body Health Capsules Recalled for Undeclared Drug

Envy Me is recalling LaBri's Body Health Atomic dietary supplement marketed for weight loss because it contains undeclared sibutramine. That is a controlled substance that was removed from the market in October 2010 for safety reasons. Sibutramine can substantially increase blood pressure and/or pulse rate in some patents and can present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias, or stroke. No reports of illness have been received to date by the company, but the FDA has reported one adverse event that occurred in June 2016. The products were sold nationwide through internet sales beginning in early 2015. Consumers should stop using the product immediately and throw it away in accordance with local ordinances for … [Read more...]

ABX Weight Loss Supplement Contains Hidden Drug

The FDA is advising consumers not to purchase or use ABX Weight Loss, a product promoted for weight loss, because it contains sibutramine, a controlled substance. There is no word on whether or not this product has been associated with any adverse effects or illnesses. Sibutramine was removed from the market in October 2010 because it substantially increases blood pressure and/or pulse rate in some people and may be a significant risk for people with heart disease. It may also interact in life-threatening ways with other medications. The product was sold at www.zxtbeepollenpills.com and may have been sold in some retail stores. If you purchased this product, do not use it. Take it to the drug disposal center in your area or return it to the place of purchase for a refund. You can … [Read more...]

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