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Dietary Supplementation News (Page 20)
Related terms: Supplementation, Dietary
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...
FDA Medwatch Alert: iFlora Kids Multi-Probiotic and iFlora 4-Kids Powder Dietary Supplements: Recall - Possible Salmonella Contamination
ISSUE: Sedona Labs today announced that its supplier of Galactooligosaccharide (GOS) has recalled this ingredient due to a possible Salmonella contamination. As a result,Sedona Labs is now...
FDA Medwatch Alert: Cataplex ACP, Cataplex C, and Pancreatrophin PMG Dietary Supplements: Recall - Potential for Contamination With Salmonella
ISSUE: Standard Process and FDA notified consumers and healthcare professionals of a recall of three dietary supplements due to potential Salmonella contamination: Cataplex ACP (Product number 0700...
FDA Medwatch Alert: Digestive 3 in 1 Health Liquid Dietary Supplement: Recall - Potential for Contamination With Salmonella
ISSUE: Botanical Laboratories Inc. and FDA notified consumers and healthcare professionals of a recall of Wellesse Digestive 3 in 1 Health liquid dietary supplement. A supplier of one of the...
FDA Medwatch Alert: West Coast Nutritionals Dietary Supplement Products: Recall - Undeclared Drug Ingredient
including: Firminite, Extra Strength Instant Hot Rod, Libidron [Posted 05/21/2012] ISSUE: West Coast Nutritionals, Ltd. is conducting a recall of all lots of their dietary supplements Firminite,...
FDA Medwatch Alert: Healthy People Co. Dietary Supplements: Recall - Undeclared Drug Ingredient
Recall includes the following products/lot numbers/UPC numbers: Mince Belle Dietary Supplement (30 Capsules) Lots HPCMB/10-026, HPCMB/10-027, HPCMB/10-029, HPCMB/10-020, HPCMB/10-021;...
FDA Medwatch Alert: Uprizing 2.0: Recall - Undeclared Drug Ingredient: Synthetic Steroid
ISSUE: FDA notified the manufacturer that lab analyses found that the product, sold as a testosterone booster, contains superdrol, a synthetic steroid, making it an unapproved new drug. Acute liver...
FDA Medwatch Alert: SimplyThick: Public Health Notification - Risk of Life-Threatening Bowel Condition
[Updated 06/05/2011] Simply Thick, LLC is announcing a voluntary recall of its SimplyThick thickening gel products manufactured at a food processing plant owned and operated by Thermo Pac, LLC. This...
FDA Medwatch Alert: Pentrexyl Forte Natural: Recall - Misleading Packaging
ISSUE: Phoenix Import & Distribution LLC and FDA notified the public of a recall for Pentrexyl Forte Natural because the packaging is believed to be misleading, causing it to be confused with an...
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