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Dietary Supplementation News (Page 21)
Related terms: Supplementation, Dietary
FDA Medwatch Alert: BEST SLIM 40 Pills By CTV Best Group: Recall - Undeclared Ingredients
ISSUE: CTV Best Group announced that it is conducting a voluntary nationwide recall of all lots of a dietary supplement products distributed by the company under the names BEST SLIM 40 Pills to the ...
FDA Medwatch Alert: Bethel Advance And Quick Thin Products By Bethel Nutritional Consulting, Inc.: Recall - Undeclared Ingredients
ISSUE: Bethel Nutritional Consulting, Inc., New York, NY, is voluntarily recalling Quick Thin and Bethel Advance to the consumer level. These products have been found to contain Sibutramine and...
FDA Medwatch Alert: Esbelin Silouttte Te and Esbelin Siloutte Vitamin Supplement: Recall - Undeclared Drug Ingredients
ISSUE: On July 19, 2013, Herbal Give Care LLC issued a voluntarily recall of all lots of Esbelin siloutte te and Esbelin siloutte Herbal Blend with L-Carnitine (30 Capsules), to the consumer level....
FDA Medwatch Alert: Oxyphen, Phentalene, Phen FX, and Red Vipers by Beta Labs, LTD: Recall - Contains DMAA
ISSUE: Beta Labs, LTD is recalling Oxyphen XR (Lot #s 200910 and 200911), Phentalene (Lot # 58800512), Phen FX (Lot # 1205129), and Red Vipers (Lot # 1205128). The recall was initiated on June 15,...
FDA Medwatch Alert: Eba Multivitamin Supplement By Saratoga Therapeutics LLC: Recall - Allergy Alert On Undeclared Milk Components
ISSUE: Saratoga Therapeutics, LLC of North Wales, PA recalled 900 bottles of ebA Multivitamin Supplement because they may contain undeclared milk components – milk protein(s) and lactose. The label l...
FDA Medwatch Alert: Ferrous Sulfate Tablets, 325 mg Labeled as Rugby Natural Iron Supplement: Recall - Bottle May Contain Meclizine HCl 25 mg Tablets
ISSUE: Advance Pharmaceutical Inc. notified the public of a recall of one lot of Ferrous Sulfate Tablets 325 mg, after notification by a pharmacist that a bottle of Ferrous Sulfate Tablets, 325 mg co...
FDA Medwatch Alert: SLIMDIA Revolution: Public Notification - Contains Undeclared Drug Ingredient Sibutramine
UPDATED 12/21/2012 P&J Trading announced today that it is conducting a voluntary nationwide recall of the company's dietary supplements sold under the brand name SLIMDIA REVOLUTION after being n...
FDA Medwatch Alert: Reumofan Plus Dietary Supplement Relabeled and Sold as “WOW”: Public Warning - Undeclared Drug Ingredients
ISSUE: The U.S. Food and Drug Administration (FDA) is warning the public that the potentially harmful dietary supplement product Reumofan Plus is being relabeled and sold under the name “WOW.” The pr...
FDA Medwatch Alert: Protandim by LifeVantage Corporation: Recall - Possible Metal Fragments in Product
ISSUE: LifeVantage Corporation announced a voluntarily recall of Protandim, the Nrf2 Synergizer dietary supplement. The Company is taking this action due to the possible inclusion of small metal...
FDA Medwatch Alert: Classic Zi Xiu Tang Bee Pollen Capsules And Ultimate Formula Capsules by Zi Xiu Tang Success: Recall - Undeclared Sibutramine
ISSUE: TZi Xiu Tang Success, LLC is voluntarily recalling four lots of Classic Zi Xiu Tang Bee Pollen Capsules, and three lots of Ultimate Formula Capsules to the consumer level. These products have...
FDA Medwatch Alert: Mojo Nights and Mojo Nights for Her: Recall - Undeclared Drug Ingredient
ISSUE: Evol Nutrition Associates, Inc./Red Dawn (“Evol Nutrition”) notified the public of a nationwide recall of all lots of two dietary supplement products distributed by the company under the names ...
FDA Medwatch Alert: SimplyThick: Public Health Notification - Risk of Life-Threatening Bowel Condition
[Updated 09/18/2012] FDA issued an advisory in May 2011 that warned of the risk to infants born prematurely. FDA is now extending that advice to include infants of any age. [Updated 06/05/2011] ...
FDA Medwatch Alert: ACTRA-Sx 500 Capsules by Body Basics Inc.: Recall - Undeclared Drug Ingredient
ISSUE: Body Basics Inc. announced that it is conducting a voluntary nationwide recall of ACTRA-Sx 500 Dietary Supplement Capsules, Lot 008-A, Expiration December 2013. The Company, through ...
FDA Medwatch Alert: EphBurn 25 Dietary Supplement by Brand New Energy: Recall - Undeclared Drug Ingredient
ISSUE: Brand New Energy and FDA notified the public of a recall of all lot codes of EphBurn 25. One lot of EphBurn 25 sampled by the FDA was found to contain ephedrine alkaloids, making it an ...
FDA Medwatch Alert: Reumofan Plus: Recall - Undeclared Drug Ingredient
[UPDATED 08/21/2012] FDA is issuing an updated alert that Reumofan Plus and Reumofan Plus Premium contain undeclared active ingredients found in prescription drugs that should be used only under the...
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Vitamins, multivitamin, l-theanine, glucose, Vitamin C, yogurt, niacin, Zinc