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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Food

NatureAll-STF Holding, LLC: Undeclared allergens: milk (Colostrum, Dried Yogurt, Whey).; Undeclared allergens: milk (Whey); Undeclared allergens: milk (Colostrum); Undeclared allergens: soy (lecithin)

Agency Publication Date: August 14, 2017
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Affected Products

Product: Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,

Lot 43200916, Exp 9/2019

Lot Numbers:
43200916
Product: Metabo-Plus, Garlic/Papaya Plus, No. 103, 90 Capsules, Dietary Supplement

Lot 39700615, Exp 6/2018

Lot Numbers:
39700615
Product: Thymus Plus, No. 114, 90 Capsules, Dietary Supplement

Lot 43701116, Exp 11/2019

Lot Numbers:
43701116
Product: Heart-Plus, No. 83, 120 Capsules, Dietary Supplement

Lot 40800915 & 44300217

Lot Numbers:
40800915
Product: Liver-Plus, No. 111 & 115, 120 Capsules, Dietary Supplement

Lot 43000816 & 45000417

Lot Numbers:
43000816
Product: Pancreas-Plus, No. 112, 90 Capsules, Dietary Supplement

Lot 42100516 & 45400517

Lot Numbers:
42100516
Product: Prostate-Plus, No. 117, 90 Capsules, Dietary Supplement

Lot 42700616

Lot Numbers:
42700616
Product: Leci-thin-Plus, No. 88, 90 Capsules, Dietary Supplement

Lot 41400116

Lot Numbers:
41400116

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 77831
Status: Resolved
Manufacturer: NatureAll-STF Holding, LLC
Manufactured In: United States
Units Affected: 8 products (367 bottles.; 254 bottles.; 107 bottles.; 598 bottles.; 400 bottles.; 566 bottles.; 186 bottles.; 80 bottles.)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.