FDA Recalls Magnesium Glycinate Gummies Over Undeclared Melatonin

The FDA issued a Class II recall for 13,920 bottles of Adndale magnesium glycinate gummies manufactured by Dkiru LLC (Dublin, Ireland) due to undeclared melatonin, with recalls announced June 19 (starting May 12) and tied to LOTs 190824, 240923, and 240929 (EXP 08/19/2026, 09/22/2026, 09/28/2026). The Cleveland Clinic notes excessive magnesium can cause GI symptoms, low blood pressure and other issues, with general daily allowances around 400 mg for men and 320 mg for women. Consumers should check the UPC 86000878455111 and the recalled lots, and dispose/return if affected.