RecallHawk
Class II Recall

Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containing 90 gummies. Net weight: 11.36 ounces. Serving size

Dkiru LLC

Summary

The FDA issued a Class II for Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containing 90 gummies by Dkiru LLC. Reason: Undeclared melatonin..

Details

Source

Food Recall

External ID

H-1079-2026

Action Date

2026-06-24

Status

Ongoing

Category

food

Product Description

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

Lot/Code Info: LOT 190824 Expiration Date: 08/19/2026, LOT 240923 Expiration Date: 09/22/2026, and LOT 240929 Expiration Date: 09/28/2026

Quantity Affected: 13,920 bottles

Reason for Recall

Undeclared melatonin.

Distribution

Will be provided when available.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-05-12

Company

Dkiru LLC

Sheridan, WY

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 47 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Dkiru LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Dkiru LLC have FDA actions?

This is the only FDA action we have on record for Dkiru LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1079-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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