Food Recall Check
Class I · High risk Terminated Initiated Jul 3, 2022 (4 years ago)

Natreve Vegan Protein Powder 10 servings recall

Recalled by Arborypharm Foods INC. · Vancouver, Canada

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

Why it was recalled

Undeclared allergen; milk.

Undeclared allergen: Milk

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

Natreve Vegan Protein Powder 10 servings, 13.1oz (371g), UPC 628831120003 18 servings, 1.47lbs/23.53oz (667g), UPC 628831110073

Quantity: 6,683 units

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.

Lot# 46359, Best Before Date: 2/2025 10 servings, 13.1oz (371g), UPC 628831120003 Lot# 46360, Best Before Date: 2/2025 18 servings, 1.47lbs/23.53oz (667g), UPC 628831110073 10 servings, 13.1oz (371g), UPC 628831120003

Where it was sold

Nationwide.

FDA's distribution note: U.S. distribution to the following: nationwide throughout the U.S. No foreign distribution.

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 milk; 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
Arborypharm Foods INC.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 3, 2022
In FDA report of
Jul 20, 2022
Terminated
Sep 29, 2022
FDA recall number
F-1428-2022 · event 90561
Official record
FDA enforcement report search