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