Import alertFDA · Apr 2, 2020
Named company: Tonic Life S de RL
DETENTION WITHOUT PHYSICAL EXAMINATION OF DIETARY SUPPLEMENT PRODUCTS FROM FIRMS THAT HAVE NOT MET DIETARY SUPPLEMENT GMP. Firm/address: Tonic Life S de RL Date Published : 04/02/2020 Calle Acambaro 1008 ,…
RecallFDA · Mar 27, 2020
Named company: CT Health Solutions, LLC
Due to different color of powder in capsules. Firm's evaluation determined product low potency.
RecallFDA · Mar 24, 2020
Named company: Alfa Vitamins Laboratories, Inc.
FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.
RecallFDA · Mar 16, 2020
Named company: Mountain Rose Inc. dba Mountain Rose Herbs
Salmonella
Warning letterFDA · Mar 6, 2020
Named company: Herbal Amy Inc
FDA has determined that these products are unapproved new drugs sold in violation of section 505(a) of the Federal Food, Drug, and Cosmetic Act (FD&C Act), 21 U.S.C. § 355(a). Furthermore, these products are…
RecallFDA · Mar 2, 2020
Named company: New Capstone, Inc
The firm was notified that the labeling does not include the word milk on the ingredient statement
RecallFDA · Feb 28, 2020
Named company: National Vitamin Company Inc
Customer reports of label error. Front panel states strength of 1000 mg although supplement fact is correct in stating 1000 mcg.
RecallFDA · Feb 24, 2020
Named company: Organic By Nature, Inc.
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
RecallFDA · Feb 24, 2020
Named company: Organic By Nature, Inc.
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop
RecallFDA · Feb 24, 2020
Named company: Organic By Nature, Inc.
Firm was notified by supplier that Organic Ground Flaxseed powder was under recall by manufacturer due to unapproved herbicide - Haloxyfop