RecallHawk
Class II Recall

2 oz VIVE ORGANIC DETOX + IMMUNITY KIWI APPLE SUPERGREENS WELLNESS SHOT; Total package size: 12 bottles per case; Stora

Vive Organic

Summary

The FDA issued a Class II for 2 oz VIVE ORGANIC DETOX + IMMUNITY KIWI APPLE SUPERGREENS WELLNESS SHOT; Total p by Vive Organic. Reason: Undeclared allergen; coconut.

Details

Source

Food Recall

External ID

F-0001-2024

Action Date

2023-10-11

Status

Terminated

Category

food

Product Description

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

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

Quantity Affected: 46,716 - 2 oz. bottles

Reason for Recall

Undeclared allergen; coconut

Distribution

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.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-09-20

Company

Vive Organic

Oceanside, CA

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 163 food recalls issued in the same week, part of 204 food-related FDA actions this month.

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 (Vive Organic) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Vive Organic have FDA actions?

This is the only FDA action we have on record for Vive Organic in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0001-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions