Food Recall Check
Class I · High risk Terminated Initiated Dec 17, 2024 (2 years ago)

Orgain recall

Recalled by Orgain, LLC · Irvine, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Potential contamination of undeclared allergen peanuts

Undeclared allergen: Peanut

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Orgain 30g Plant Protein, Complete Protein Powder, 6g Prebiotic +Fiber, 9g EAAS+BCAAs, 1gSugar, Chocolate Flavor; NET WT 32.1 OZ (2.01 LB) 912g; Nutritional Facts: Serving size 2 scoops, UPC: 8 51770 00760 3; QUESTIONS ABOUT ORGAIN PRODUCTS? 888-881-GAIN(4246) Lot# 4172-02-P

Quantity: 523 cases (12 count/case)

Food: Chocolate & candy

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Expiration date: 06-20-26

Where it was sold

FDA's distribution note: Direct account list is still being compiled by firm. Customers include other than domestic. 6 total direct accounts( 4 distributors, 2 retail)

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to peanut; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Orgain, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 17, 2024
In FDA report of
Jan 22, 2025
Terminated
May 20, 2025
FDA recall number
F-0386-2025 · event 96021
Official record
FDA enforcement report search

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