FDA recall record

THGH Partners Power Life by Tony Horton High Impact Plant Protein Chocolate recall — FDA F-0216-2023

Incorrect product label causing undeclared milk.

Class Iclassification
F-0216-2023official record ID
Jan 11, 2023report date

Recall record at a glance

Official recordF-0216-2023
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmTHGH Partners, LLC
Report dateJan 11, 2023
Recall initiation dateDec 5, 2022
Quantity6,782 units
LocationCalabasas, CA, United States

Official product description

Power Life by Tony Horton High Impact Plant Protein Chocolate Flavor NET WT 446 G (15.7 OZ) Ingredients: Vegan Protein Mix (pumpkin, sunflower, flax)(as ProteoSMART), Mung Bean Protein, myHMB (Calcium Beta-hydroxy-Beta-Methlbutyrate), Alkalized Cocoa Powder, Pea Protein Powder, Gum Blend (guar gum, xanthan gum), Pink Himalayan Sea Salt, Natural Flavor, Chlorella protothecoides (as AlgaRich vegi-PSS), Digestive Enzyme Blend (Bacillus subtilis, Ananas comosus)(as ProHydrolase). Monk Fruit Extract, Vitamin D3 (plant source) (as VegD3), Chromium Picolinate (as Chromax) Contains Gluten (from Wheat) and Soy (soy and wheat are used in the microbial fermentation of the ProHydrolase enzyme BUT not added into the product). Distributed by Power Life Nutrition 4500 Park Granada Boulevard, Suite 200 Calabasas, CA 91302 855-462-2496 MyPowerLife.com UPC 8 50010 86301 6

Why the product was recalled

Incorrect product label causing undeclared milk.

Distribution information

Product was sold online only in the United States, United Kingdom, Australia, New Zealand, Canada, and Mexico.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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