Food Recall Check
Class II · Moderate risk Terminated Initiated Sep 20, 2023 (3 years ago)

2 oz VIVE ORGANIC DETOX + IMMUNITY KIWI APPLE SUPERGREENS WELLNESS SHOT recall

Recalled by Vive Organic · Oceanside, CA, United States

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

Why it was recalled

Undeclared allergen; coconut

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

2 oz VIVE ORGANIC DETOX + IMMUNITY KIWI APPLE SUPERGREENS WELLNESS SHOT; Total package size: 12 bottles per case; Storage instructions: Keep Refrigerated; Date(s) of manufacture: 06/29/23 - 06/30/23

Quantity: 46,716 - 2 oz. bottles

Food: Fresh fruit

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.

Best By Date: 12/10/23 - O; UPC 856502006855

Where it was sold

Arizona California Colorado Connecticut Florida Georgia Iowa Illinois Indiana Maryland New York Pennsylvania Texas Utah Washington Wisconsin

FDA's distribution note: Vive Organic did not sell directly to any consignees. Vive Organic did not sell directly to any wholesale dealers. TOTAL number of distributors that received the recall product = 12. TOTAL number of retailers that received the recall product = 10. U.S. distribution to: AZ, CA, CO, CT, FL, GA, IA, IL, IN, MD, NY, PA, TX, UT, WA, WI. No foreign distribution.

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
Vive Organic
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 20, 2023
In FDA report of
Oct 11, 2023
Terminated
Dec 19, 2023
FDA recall number
F-0001-2024 · event 93117
Official record
FDA enforcement report search

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