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Dietary Supplementation News (Page 18)
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FDA Medwatch Alert: 8th Avenue Pharmacy Issues Voluntary Nationwide Recall of Notoginseng Formula Special Gout Granule Due to the Presence of Hidden Drug Ingredients, Diclofenac and Dexamethasone
December 14, 2023 – Brooklyn, NY, 8th Avenue Pharmacy is voluntarily recalling all lots within expiry of Notoginseng Formula Special Gout Granule, distributed by 8th Avenue Pharmacy, to the consumer...
FDA Medwatch Alert: Noah’s Wholesale, LLC Issues Voluntary Nationwide Recall of the Rock Due to Presence of Undeclared Sildenafil
October 18, 2023 – Miami Gardens, Florida, Noah’s Wholesale, LLC is voluntarily recalling one lot of the rock# 03032021,exp:12/2027,1200 mg/capsule, to the consumer level. FDA analysis has found the p...
FDA Medwatch Alert: FDA Warns Consumers Not To Purchase or Use Neptune’s Fix or Any Tianeptine Product Due To Serious Risks
November 21, 2023 – FDA is warning consumers to not purchase or use any Neptune’s Fix products, or any other product with tianeptine – a potentially dangerous substance that is not FDA-approved for ...
FDA Medwatch Alert: FDA Raises Concerns About Probiotic Products Sold for Use in Hospitalized Preterm Infants
October 26, 2023 – As part of the U.S. Food and Drug Administration’s commitment to protecting public health, the agency is advising the public, including healthcare providers, of the possible risks ...
FDA Medwatch Alert: Botanical-Be Issues Voluntary Nationwide Recall of Kuka Flex Forte, Artri King, and Reumo Flex (Capsules) Due to Presence of Undeclared Diclofenac
October 22, 2023 – El Paso, TX. Botanical-Be is voluntarily recalling of all lots of Kuka Flex Forte, Capsules, Artri King, Capsules, and Reumo Flex, Capsules to the consumer level. FDA analysis has f...
FDA Medwatch Alert: Warning Regarding Use of Probiotics in Preterm Infants
September 29, 2023 – The U.S. Food and Drug Administration (FDA) is providing important safety information to healthcare providers on the use of products containing live bacteria or yeast (commonly...
FDA Medwatch Alert: WEFUN Inc. Issues Voluntary Nationwide Recall of WEFUN Capsules Due to Presence of Undeclared Sildenafil
Brooklyn, New York, WEFUN Inc. is voluntarily recalling 300 Boxes of WEFUN Capsules to the consumer level. FDA analysis has found the product to be tainted with sildenafil. Sildenafil is an...
FDA Medwatch Alert: Volt Candy Issues Voluntary Nationwide Recall of PrimeZen Black 6000 Capsules Due to Presence of Sildenafil and Tadalafil
February 7, 2023 -- The Food and Drug Administration is advising consumers not to purchase or use PrimeZen Black 6000, a product promoted and sold for sexual enhancement on various websites, ...
FDA Medwatch Alert: Public Notification: Alfia Weight Loss Capsules Contain Hidden Drug Ingredient
February 8, 2023 -- The Food and Drug Administration is advising consumers not to purchase or use Alfia Weight Loss Capsules, a product promoted and sold for weight loss on various websites ...
FDA Medwatch Alert: FDA Warns Seven Companies for Selling Dietary Supplements with Claims to Treat Cardiovascular Disease
November 17, 2022 – Today, the U.S. Food and Drug Administration issued warning letters to seven companies for illegally selling dietary supplements that claim to cure, treat, mitigate or prevent...
FDA Medwatch Alert: Proper Trade LLC/My Stellar Lifestyle Issues Voluntary Nationwide Recall of Wonder Pill Capsules Due to the Presence of Undeclared Tadalafil
September 28, 2022 – Proper Trade LLC/My Stellar Lifestyle is voluntarily recalling Wonder Pill lot 20210912 and lot 31853-501, expiry 09/24, packaged in 10-count blisters co-packaged in a carton...
FDA Medwatch Alert: Distributor RFR, LLC, Voluntary Nationwide Recall of Sangter Energy Supplement Due to Presence of Undeclared Sildenafil
August 1, 2022 – Miami, Florida, DISTRIBUTOR RFR, LLC. is voluntarily recalling lot #48656, Exp. 01/2025 of SANGTER Energy Supplement, 3000 mg, packaged in 7-count blister packs within a carton to t...
FDA Medwatch Alert: Loud Muscle Science, LLC Issues Voluntary Recall of Launch Sequence Capsules Due to the Presence of Undeclared Tadalafil in United States and Canada
July 26, 2022 – Hauppauge, NY, Loud Muscle Science, LLC is voluntarily recalling the following Launch Sequence products and lots listed in the table below to the consumer level. Laboratory analysis...
FDA Medwatch Alert: Ultra Supplement LLC Issues Voluntary Nationwide Recall of Sustango Due to the Presence of Undeclared Tadalafil
July 21, 2022 -- Wilmington DE, Ultra Supplement LLC is voluntarily recalling lot number DAP272109, exp 4/1/26 of Sustango capsules packaged in 10-count blisters packaged in a carton to the consumer ...
FDA Medwatch Alert: Latin Foods Market Issues Voluntary Nationwide Recall of Artri King Reforzado Con Ortiga Y Omega 3 Due to the Presence of Undeclared Diclofenac and Dexamethasone
June 14, 2022 – Latin Foods Market is voluntarily recalling one lot, LOTE 334 21, of Artri King Reforzado con Ortiga y Omega 3 tablets to the consumer level. FDA analysis has found the product to be...
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