Revie Superfoods Heart Beet 206g Ready-to-Blend Cardamom + Beet Smoothie Made in Canada UPC 8 53267 00112 5 Revive
Summary
The FDA issued a Class II for Revie Superfoods Heart Beet 206g Ready-to-Blend Cardamom + Beet Smoothie Made by Revive Organics, Inc.. Reason: Potential norovirus from IQF raspberries that were used as an ingredient in the products..
Details
Source
Food Recall
External ID
F-1433-2022
Action Date
2022-07-27
Status
Terminated
Category
food
Product Description
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
Lot/Code Info: Lot numbers -1010422, 1090422, 1100422, 1260522, 1290522, 1320522, 1180422, 1020422, 1110422, 1230522, 1030422, 1170422, 1250522, 1240522
Quantity Affected: 57,960 units (total)
Reason for Recall
Potential norovirus from IQF raspberries that were used as an ingredient in the products.
Distribution
U.S. distribution to distributors located in PA, CA, IL, and TX who further distributed directly to consumers.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-06-11
Company
Oakville, N/A
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 88 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Revive Organics, Inc. has 7 FDA actions in our database, including 7 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Revive Organics, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Revive Organics, Inc. have FDA actions?
Revive Organics, Inc. has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1433-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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