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ActiPharma, Inc.

1 recalls on record

This page lists all FDA food recalls initiated by ActiPharma, Inc.. Data is sourced directly from the FDA enforcement database and updated weekly. Class I recalls indicate the most serious health risk.

FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid spe
Class III2023-09-28#F-0463-2024

Browse by recall reason

ListeriaSalmonellaE. coliUndeclared allergensPeanutUndeclared milkWheat / glutenForeign materialMetal contaminationGlass contaminationPlastic contaminationMold / spoilageLabeling errorsHepatitis ANorovirus