RecallHawk
Class I Recall

Power Life by Tony Horton High Impact Plant Protein Chocolate Flavor NET WT 446 G (15.7 OZ) Ingredients: Vegan Protein

THGH Partners, LLC

Summary

The FDA issued a Class I for Power Life by Tony Horton High Impact Plant Protein Chocolate Flavor NET WT 446 by THGH Partners, LLC. Reason: Incorrect product label causing undeclared milk..

Details

Source

Food Recall

External ID

F-0216-2023

Action Date

2023-01-11

Status

Terminated

Category

food

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

Lot/Code Info: lot 0914922

Quantity Affected: 6,782 units

Reason for Recall

Incorrect product label causing undeclared milk.

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2022-12-05

Company

THGH Partners, LLC

Calabasas, CA

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (THGH Partners, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does THGH Partners, LLC have FDA actions?

This is the only FDA action we have on record for THGH Partners, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0216-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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