Power Life by Tony Horton High Impact Plant Protein Chocolate Flavor NET WT 446 G (15.7 OZ) Ingredients: Vegan Protei... — FDA record F-0216-2023

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 5, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
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
Reason
Incorrect product label causing undeclared milk.
Classification
Class I
Recalling firm
THGH Partners, LLC
Quantity
6,782 units
Agency-reported status
Terminated
Source record identifier
F-0216-2023

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilitylot 0914922

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

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

No US distribution state could be established from this record. Check the official notice.

Dates in the source

Report date
Jan 11, 2023
Recall initiation date
Dec 5, 2022
Center classification date
Jan 5, 2023
Termination date
Jan 10, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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