What happened
Original notice title
Deggeh Foods, Inc. MARCS-CMS 628460, July 29, 2022
From the archived source record
Based on our inspection and subsequent review of product labeling collected during the inspection, your firm’s website at the Internet address [see original source] and your Facebook social media page at [see original source] category /Community/Deggeh-products-Natural-Organic-products-made-in-Gambia-564035160361406/, we have identified serious violations of the Federal Food, Drug, and Cosmetic Act (the Act) and applicable regulations. Unapproved New Drugs and Misbranded Drugs FDA reviewed your website at the Internet address [see original source] in June 2022 and has determined that you take orders there for your products Actibest® Health Plus Capsules, Best Hemorrhoids Rapid Action Herbal Healing Formula, StomachAID capsules, and Moringa Tea Bags. Food Poisoning Stomach Worms & Parasites” Best Hemorrhoids Rapid Action Herbal Healing Formula Product Label: “Best Hemorrhoids Rapid Action Herbal Healing Formula” Moringa Tea Bags Product Label: “Get almost instant results and relief for: MIGRAINS [sic], HIGHBLOOD [sic] PRESSURE, HIGH SUGAR, DIABETES, HIGH CHOLESTEROL . . . A drug is misbranded under section 502(f)(1) of the Act [21 U.S.C. 352(f)(1)] if the drug fails to bear adequate directions for its intended use(s). Accordingly, Actibest® Health Plus Capsules, StomachAID capsules, and Moringa Tea Bags fail to bear adequate directions for their intended use and, therefore, the products are misbranded under section 502(f)(1) of the Act [21 U.S.C. 352(f)(1)]. The introduction or delivery for introduction into interstate commerce of these misbranded drugs violates section 301(a) of the Act [21 U.S.C. 331(a)]. Adulterated Dietary Supplements The facility inspection revealed serious violations of the FDA’s regulations for Current Good Manufacturing Practice (CGMP) in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements, under Title 21, Code of Federal Regulations (CFR), Part 111 (21 CFR Part 111).
What the official notice says to do
Check the original notice for the instructions that apply to the named product, company, and affected lots.
Read the official notice →Status and source details
- Status recorded in the archive
- No closeout listed in FDA table
- Source checked
- Jul 16, 2026
- Record revision
- 547ee4c8d3c8
This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.
Sources, dates, and coverage →