ActiPharma, Inc. is recalling 607 bottles of ACTIRON Dietary Supplement (100 tablets per bottle) because FDA testing revealed the product contains less folic acid than the amount claimed on the label. This folic acid deficiency was discovered during sample analysis of lot 13309. No incidents or injuries have been reported to date regarding this recall.
The supplement does not meet the potency specifications for folic acid listed on the label, meaning consumers are not receiving the nutritional amount promised on the packaging.
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Distributed in cases of 24 bottles per case.
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Sources: FDA iRES · Raw API Response
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