RecallFDA · Aug 28, 2019
Named company: Jivan Shakti Inc.
Product label declares Vitamin D3 at 200 IU per serving. FDA sample analysis revealed no Vitamin D in product.
RecallFDA · Jul 30, 2019
Named company: Green Water, LLC
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea, Mothers Milk Tea…
RecallFDA · Jul 30, 2019
Named company: Green Water, LLC
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea, Mothers Milk Tea…
RecallFDA · Jul 30, 2019
Named company: Green Water, LLC
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea, Mothers Milk Tea…
RecallFDA · Jul 30, 2019
Named company: Green Water, LLC
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea, Mother s Milk Tea…
RecallFDA · Jul 30, 2019
Named company: Green Water, LLC
recalling certain lots of Bedroom Bliss Herbal Tincture, Breathe Easy Herbal Tincture, Digest Ease Herbal Tincture, Happy Momma Herbal Tincture, Mojo Magic Herbal Tincture, Respiratory Tea, Mothers Milk Tea…
Public notificationFDA · Jul 22, 2019
Named company: Curaleaf, Inc.
Unapproved New Drugs/Misbranded/Cannabidiol (CBD) Products
RecallFDA · Jul 9, 2019
Named company: FoodScience Corporation
Dietary supplement mislabeled, undeclared allergen.
Import alertFDA · Jun 26, 2019
Named company: EXPO CONNECT SDN BHD
"DETENTION WITHOUT PHYSICAL EXAMINATION OF PRODUCTS THAT ARE MARKETED AS FOODS, INCLUDING PRODUCTS MARKETED AS DIETARY SUPPLEMENTS, THAT CONTAIN AN ACTIVE PHARMACEUTICAL INGREDIENT". Firm/address: EXPO CONNECT…
Warning letterFDA · Jun 25, 2019
Named company: Cali Botanicals, LLC
FDA has determined that these products are unapproved new drugs sold in violation of sections 505(a) and 301(d) of the Federal Food, Drug, and Cosmetic Act ( FD&C Act), 21 U.S.C. 355(a) and 331(d).…