Skip to main content

Dietary Supplementation News (Page 21)

Related terms: Supplementation, Dietary

FDA Medwatch Alert: Compounded Multivitamins by Glades Drugs: Voluntary Recall - High Amounts of Vitamin D3 (Cholecalciferol)

ISSUE: The U.S. Food and Drug Administration is alerting health care professionals and patients of a voluntary recall of compounded multivitamin capsules containing high amounts of Vitamin D3...

FDA Medwatch Alert: Ayurvedic Dietary Supplements by Shree Baidyanath: Consumer Advice Notice - Products Contain High Levels of Lead and/or Mercury

[Posted 09/17/2015] ISSUE: Consumers who have used any of the Baidyanath brand Ayurvedic dietary supplements listed in the Consumer Advice Notice should stop using them and consult their health care...

FDA Medwatch Alert: Mayhem: Public Notification - Undeclared Drug Ingredients

ISSUE: FDA is advising consumers not to purchase or use Mayhem, a product labeled as a dietary supplement that is promoted to increase appetite and muscle growth, because it contains an undeclared...

FDA Medwatch Alert: V26 Slimming Coffee: Public Notification - Undeclared Drug Ingredient

ISSUE:  FDA is advising consumers not to purchase or use V26 Slimming Coffee. FDA laboratory analysis confirmed that V26 Slimming Coffee contains sibutramine. Sibutramine is a controlled substance ...

FDA Medwatch Alert: RegeneSlim Appetite Control Capsules: Recall - Presence Of DMAA

UPDATED 09/02/2014. Voluntary nationwide recall expanded to include lot #823230415, lot #EX0616r 15813, Lot # EX0616R15814, and Lot #11414re5516. [Posted 08/07/2014] ISSUE: Regeneca Worldwide a...

FDA Medwatch Alert: RegeneSlim Appetite Control Capsules: Recall - Presence Of DMAA

[Posted 08/07/2014] ISSUE: Regeneca Worldwide a division of VivaCeuticals, Inc., is conducting a voluntary nationwide recall of its appetite control dietary supplement, lot # EX0616R15814 and lot...

FDA Medwatch Alert: L-citrulline by Medisca: Alert - Potentially Subpotent Product

UPDATED 02/17/2014. FDA has tested samples from recalled lots of Medisca’s L-citrulline product, and were analyzed by several laboratory methods to identify the ingredient that was repackaged by M...

FDA Medwatch Alert: Muscle Growth Product Called Mass Destruction: FDA Health Risk Warning - Undeclared Ingredients

ISSUE: The FDA is advising consumers to immediately stop using a product called Mass Destruction, marketed as a dietary supplement for muscle growth. The product is labeled to contain at least one...

FDA Medwatch Alert: OxyElite Pro Dietary Supplements by USP Labs: Recall - Products Linked to Liver Illnesses

ISSUE: The U.S. Food and Drug Administration announced today that USPlabs LLC, of Dallas, Texas, is recalling certain OxyElite Pro dietary supplement products that the company markets. The company...

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...

Ask a question

To post your own question to our community, sign in or create an account.

Further information

Related drug support groups

Vitamins, multivitamin, l-theanine, glucose, Vitamin C, yogurt, niacin, Zinc