Food recall

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

Vive Organic, of Oceanside, CA, recalled 2 oz VIVE ORGANIC DETOX + IMMUNITY KIWI APPLE SUPERGREENS WELLNESS SHOT. The FDA's reason: “Undeclared allergen; coconut.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on September 20, 2023, and the FDA first listed it in its Enforcement Report of October 11, 2023. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.

How serious

Class II

It could cause temporary or minor harm

Why

Allergen not on the label

Status

Terminated

Closed December 19, 2023

The recall

Company
Vive Organic (Oceanside, CA)
Reason, in FDA's words
“Undeclared allergen; coconut”
Where it was sold
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.
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
93117

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • F-0001-2024 Class II

    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

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

    Quantity: 46,716 - 2 oz. bottles

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of October 11, 2023.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.