What happened
Original notice title
Plantacea, LLC dba Kahm MARCS-CMS 623508, May 26, 2022
From the archived source record
The claims on your website and social media websites establish that your products “CBD Hemp Pellets” and “K9 Soft Chews,” which you promote as products containing CBD for use in animals, are unapproved new animal drugs that are unsafe under section 512(a) of the Federal Food, Drug, and Cosmetic Act (the FD&C Act), 21 U.S.C. 360b(a), and adulterated under section 501(a)(5) of the FD&C Act, 21 U.S.C. 351(a)(5). In addition, your CBD products for human use, “Kahm EQUIPASS RELIEF GEL,” “Kahm CBD MUSCLE FREEZE ROLL ON,” “Kahm BODY CREAM,” “Kahm CBD BROAD SPECTRUM HEMP EXTRACT” (all varieties), and “Kahm CBD NANO CBD SALVE” (hereinafter “Kahm CBD products for humans”), as well as your “Tanka 30 day CBD Band,” “Tanka T-FLEX Band” and “Tanka Collagen Band,” with respect to their ingredients intended for delivery through the skin (hereinafter “Tanka products for humans”), are unapproved new drugs sold in violation of sections 505(a) and 301(d) of the FD&C Act, 21 U.S.C. 355(a) and 331(d). Furthermore, your Kahm CBD products for humans and Tanka products for humans are misbranded drugs under section 502(f)(1) of the FD&C Act, 21 U.S.C. 352(f)(1). FDA has also determined that your CBD Gummies products in Blue Raspberry and Raspberry flavors are adulterated under section 402(a)(2)(C)(i) of the FD&C Act, 21 U.S.C. 342(a)(2)(C)(i), because they bear or contain an unsafe food additive. The Agency is particularly concerned that you market CBD products for food-producing animals. In addition to raising potential concerns regarding safety for the animals themselves, CBD products for food-producing animals raise concerns regarding the safety of the human food (meat, milk, and eggs) derived from those animals. We request that you take immediate action to cease the sale of any unapproved CBD products for food-producing animals.
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
- 9d352ba0ccc8
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.
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