Warning letterFDA · May 12, 2017
Named company: Formulife, Inc.
During this inspection, our investigators found a number of violations of the current Good Manufacturing Practice (cGMP) in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements…
RecallFDA · May 8, 2017
Named company: GnuPharma Corp.
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
RecallFDA · May 8, 2017
Named company: GnuPharma Corp.
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
RecallFDA · May 8, 2017
Named company: GnuPharma Corp.
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
RecallFDA · May 8, 2017
Named company: GnuPharma Corp.
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
RecallFDA · May 8, 2017
Named company: GnuPharma Corp.
1 ingredient failed identity testing and 2 ingredients failed microbiological testing (E.coli)
RecallFDA · May 8, 2017
Named company: RB Manufacturing LLC
RB Manufacturing is recalling Move Free Advance Tablets due to incorrect packaging.
Import alertFDA · May 4, 2017
Named company: Natural Elixirs
"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: Natural…
Warning letterFDA · May 3, 2017
Named company: MS Bionic
Based on our inspection and review of your product labels, we have found serious violations of the Federal Food, Drug, and Cosmetic Act (the Act) and applicable regulations. Unapproved New Drugs FDA obtained a…
Warning letterFDA · May 1, 2017
Named company: Nature's Vision, Inc
Based on the inspection, a review of the product labeling you provided during the inspection, and our subsequent review of your website www.naturesvisioninc.com, we found serious violations of the Federal…