Fresh Recalls

FDAClass II · Food · Recall H-1079-2026 · Recalled June 24, 2026

Adndale Magnesium Glycinate Gummies 400 mg recall — Dkiru LLC

Agency report date: June 24, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Adndale Magnesium Glycinate Gummies 400 mg
Company / brand
Dkiru
Lot / serial / date codes
LOT 190824 Expiration Date: 08/19/2026, LOT 240923 Expiration Date: 09/22/2026, and LOT 240929 Expiration Date: 09/28/2026
Distribution
Will be provided when available.
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Undeclared melatonin.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: Adndale Magnesium Glycinate Gummies 400 mg

3. Open the official notice or contact

Official recall ID
H-1079-2026
Brand
Dkiru
Classification
Class II
Units affected
13,920 bottles
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Sheridan, WY, United States
Firm address
1309 Coffeen Ave Ste 1200, 82801-5777

Identifying details (verbatim from the notice)

Product codes / lots
LOT 190824 Expiration Date: 08/19/2026, LOT 240923 Expiration Date: 09/22/2026, and LOT 240929 Expiration Date: 09/28/2026
Distribution
Will be provided when available.
Firm notified the public via
E-Mail
FDA event ID
98984
Recall initiated
May 12, 2026
FDA classified
June 18, 2026
FDA report date
June 24, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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