Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containi…

Dkiru LLC has recalled Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containi…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on June 24, 2026 and was initiated on May 12, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containi…, with approximately 13,920 bottles affected. The company behind the recall is Dkiru LLC, based in Sheridan, WY. The FDA describes the product as: “Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containing 90 gummies. Net weight: 11.36 ounces. Serving size: 2 gummies. UPC: 860008784551 Firm name and address listed on label: Dkiru Ltd, Keepers Cottage, 3 Dublin Rd, Leixlip, Co. Kildare W23 H3C…”

Why was Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containi… recalled?

According to the FDA, the stated reason for the recall is: “Undeclared melatonin.” In plain terms, this recall relates to an undeclared ingredient or allergen.

An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.

What should you do?

If you think you may have bought Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containi…, compare it against the product description and identifying codes (LOT 190824 Expiration Date: 08/19/2026, LOT 240923 Expiration Date: 09/22/2026, and LOT 240929 Expiration Date: 09/28/2026) before using it. This recall is currently listed as ongoing.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Dkiru LLC or your local health authority.

About this recall

This recall was distributed in WY. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.