Adndale magnesium glycinate gummies contain undeclared melatonin in three lots
Adndale Magnesium Glycinate Gummies 400 mg are being recalled because of undeclared melatonin. The action covers 13,920 bottles.
The agency’s classification
FDA (Food): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Risk-of-harm product containing an undeclared active ingredient that consumers could take unknowingly, with no injuries reported in the source.
Plain-English summary
Adndale Magnesium Glycinate Gummies 400 mg, in a plastic bottle containing 90 gummies, net weight 11.36 ounces, UPC 860008784551, are being recalled. The label lists Dkiru Ltd. The action covers 13,920 bottles.
The stated reason is undeclared melatonin. The FDA classified the action as Class II.
Affected lots are 190824 (expiring 08/19/2026), 240923 (expiring 09/22/2026) and 240929 (expiring 09/28/2026). The recall notice states distribution information will be provided when available.
Consumers who have an affected lot should stop taking the gummies and follow the instructions issued by the firm. Anyone who has taken them and feels unwell should seek medical advice.
The recalled product
- Product
- 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
- Manufacturer
- Dkiru LLC
- Category
- Food — Dietary supplement
- Affected units
- 13,920
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- LOT 190824 Expiration Date: 08/19/2026
- LOT 240923 Expiration Date: 09/22/2026
- and LOT 240929 Expiration Date: 09/28/2026
Distribution
Distribution scope not specified by the agency.
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