Class IIOngoing in FDA datasetRecall initiated May 12, 2026

Adndale Magnesium Glycinate Gummies 400 mg. Plastic bottle containing 90 gummies. Net weight:…

Recalling firm: Dkiru LLC

Why it was recalled

Undeclared melatonin.

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Compare the exact product and package details with the label you have.

ProductAdndale 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
Package size11.36 ounces
UPC860008784551

FDA code information

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

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Full FDA record and distribution details

Original 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

Extracted codes and context

TypeCode / valueContext
UPC860008784551 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
expiration08/19/2026LOT 190824 Expiration Date: 08/19/2026, LOT 240923 Expiration Date: 09/22/2026, and LOT 240929 Expiration Date: 09/28/2026
expiration09/22/2026LOT 190824 Expiration Date: 08/19/2026, LOT 240923 Expiration Date: 09/22/2026, and LOT 240929 Expiration Date: 09/28/2026
expiration09/28/20262026, LOT 240923 Expiration Date: 09/22/2026, and LOT 240929 Expiration Date: 09/28/2026

Original FDA recall reason

Undeclared melatonin.

Recall details

Recall number
H-1079-2026
Event ID
98984
FDA status
Ongoing
Initiated
May 12, 2026
Reported
Jun 24, 2026
Classified
Jun 18, 2026
Quantity
13,920 bottles
Location
Sheridan, WY, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

Will be provided when available.

FDA source record · H-1079-2026

Data updated September 16, 2026. View official FDA data ↗

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