Recall Radar

Dkiru recalls Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle…: allergen risk

June 24, 2026 · Dkiru Class II

Class IIFDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Reason for the recallUndeclared melatonin.

Find the official FDA enforcement report

Recall at a glance

Recalling company
Dkiru
Location
Sheridan, WY
Reported by FDA
June 24, 2026
Recall started
May 12, 2026
Risk class
Class II
Status (latest data we have)
Ongoing
Type
Voluntary: Firm initiated
Category
Supplements and infant formula
Reason type
Undeclared allergens

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • 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 H3C4, Ireland
    Quantity: 13,920 bottles
    Codes: LOT 190824 Expiration Date: 08/19/2026, LOT 240923 Expiration Date: 09/22/2026, and LOT 240929 Expiration Date: 09/28/2026

Where it was distributed

Will be provided when available.

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

Dkiru recalled 1 product, including Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containing 90 gummies. Net weight: 11.36 ounces. Serving size: 2 gummies. UPC….

Why was it recalled?

Undeclared melatonin.

What does Class II mean?

FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.

Where was it sold or shipped?

Will be provided when available.

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

Similar recalls in supplements and infant formula

Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.