Revie Superfoods Heart Beet recall

Recalled by Revive Organics, Inc. · Oakville, N/A, Canada

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Potential norovirus from IQF raspberries that were used as an ingredient in the products.

A highly contagious virus, often linked to shellfish and fresh produce.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Revie Superfoods Heart Beet 206g Ready-to-Blend Cardamom + Beet Smoothie Made in Canada UPC 8 53267 00112 5 Revive Superfoods 1880 Bonhill Road, Mississauga, Ontario, Canada

Quantity: 57,960 units (total)

Food: Juice & beverages

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 numbers -1010422, 1090422, 1100422, 1260522, 1290522, 1320522, 1180422, 1020422, 1110422, 1230522, 1030422, 1170422, 1250522, 1240522

Where it was sold

California Illinois Pennsylvania Texas

FDA's distribution note: U.S. distribution to distributors located in PA, CA, IL, and TX who further distributed directly to consumers.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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: Revive Organics, Inc.
Initiated by: Voluntary: Firm initiated
Recall initiated: Jun 11, 2022
In FDA report of: Jul 27, 2022
Terminated: Feb 28, 2023
FDA recall number: F-1433-2022 · event 90517
Official record: FDA enforcement report search

Also recalled with it (6 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Norovirus Jun 11, 2022