Alert

Limbrel Capsules by Primus Pharmaceuticals: FDA Advisory – Linked to Potentially Life-Threatening Health Problems

In total, the FDA has received 194 adverse event reports regarding Limbrel, of those, 57 of the cases contained sufficient information to analyze in detail whether Limbrel was associated with an adverse event; 30 of these contained sufficient information to use the Council for International Organizations of Medical Sciences (CIOMS) causality assessment method to determine the likelihood that an association between the consumption of Limbrel and the adverse events reported exists.

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Hardcore Formulations Issues Voluntary Nationwide Recall of Ultra-Sten and D-Zine Capsules Due to Labeling that it Contains Anabolic Steroids

June 29, 2017 This is a reprint of an FDA Alert. When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company’s announcement as a public service. FDA does not endorse either the product or the company. For Immediate Release Contact Consumers sales@hardcoreformulations.com 1-855-773-6826 San Marcos, TX, Hardcore Formulations is…

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A&H Focal Inc. Issues Nationwide Recall of 21 Products Marketed as Dietary Supplements & One Cosmetic Product Due to Undeclared Drug Ingredients

This is a reprint of an FDA Alert. March 7, 2017 Contact Consumers Henry Choo: (646)327-8522 A&H Focal Inc. is voluntarily recalling all lots of the following products because many of these products have been historically tested by the FDA and found to contain PDE-5 Inhibitors (i.e. sildenafil, tadalafil, vardenafil, etc.) which is the active…

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FDA Alert: Kingsway Trading Inc. Recalls “Xanthium & Siler Combo (Bi Yan Pian) Dietary Supplement” because it Contains Banned Ephedra Alkaloids

This is a reprint of an FDA Alert. When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company’s announcement as a public service. FDA does not endorse either the product or the company. For Immediate Release February 7, 2017 Contact Consumers (718)366-2300 Kingsway Trading Inc. of Brooklyn, NY is…

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Love My Tru Body Issues Voluntary Nationwide Recall of Skinny Bee Diet Due To Presence of Undeclared Sibutramine, Desmethylsibutramine and/Phenolphthalein

This is a reprint of an FDA Alert. When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company’s announcement as a public service. FDA does not endorse either the product or the company. For Immediate Release November 8, 2016 Contact Consumers Sharon Demps lovemytrubody@yahoo.com (800) 540-7515 Company Announcement McDonough,…

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Ton Shen Health Recalls “DHZC-2 Tablet” Because of Possible Health Risk

This is a reprint of an FDA Alert. For Immediate Release August 11, 2016 Contact Consumers Ton Shen Health 1-312-842-2775 When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company’s announcement as a public service. FDA does not endorse either the product or the company. Ton Shen Health of…

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FDA Alert: The Body Shot Bar Issues Voluntary Nationwide Recall of Step 2 Due to Undeclared Sibutramine

This is a reprint of an FDA Alert. Company Announcement When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company’s announcement as a public service. FDA does not endorse either the product or the company. For Immediate Release: June 7, 2016 Contact Consumers: thebodyshotbarinfo@yahoo.com, (910)-849-3348 Media: Tiffany Braswell (910)-849-3348 The Body Shot Bar is…

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Beware of Illegally Marketed Diabetes Treatments

This is a reprint of an FDA Alert. En Español As the number of people diagnosed with diabetes continues to grow, illegally marketed products promising to prevent, treat, and even cure diabetes are flooding the marketplace. The U.S. Food and Drug Administration (FDA) is advising consumers not to use such products—for many reasons. For example,…

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