Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containi…
Recalled by Dkiru LLC
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
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.
Who this recall affects
This recall matters most to anyone with a food allergy or sensitivity to the ingredient that wasn't listed on the label. For everyone else this product is generally safe to eat — the danger is specific to people avoiding that ingredient, who had no way to know it was there.
Distribution listed in the notice: Will be provided when available..
What undeclared ingredient or allergen actually means
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.
In this case, the concern applies specifically to Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containi… from Dkiru LLC — not to the wider category of products. Similar items from other brands aren't part of this recall.
How to check whether you have it
On packaged food, lot codes and best-by dates are usually printed in small date-coding ink on the side seam, the bottom of the package, or near the top seal — not on the front label. The UPC barcode is on the back or bottom.
Compare what you find against the identifying details in this recall: LOT 190824 Expiration Date: 08/19/2026, LOT 240923 Expiration Date: 09/22/2026, and LOT 240929 Expiration Date: 09/28/2026
What to do if you already bought it
Do not eat the product, even if it looks and smells normal — contamination is usually invisible.
Return it to the store for a refund, or throw it away in a sealed bag so pets and wildlife can't reach it.
If it touched other food or surfaces, wash those surfaces and your hands with hot soapy water. When in doubt, contact Dkiru LLC or your local health department.
Full recall details
- Status
- Ongoing
- Date reported
- June 24, 2026
- Recall started
- May 12, 2026
- Distributed in
- WY
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containi… recalled?+
According to the FDA: Undeclared melatonin.
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containi…?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-1079-2026. Information last synced from the FDA on August 20, 2026.