RecallHawk
Class III Recall

Zydot Ultimate Blend The Original Detox Drink Natural Tropical Ice Flavor 16 fl. oz. (473 ml) UPC packaged in plastic bo

Zydot Unlimited, Inc

Summary

The FDA issued a Class III for Zydot Ultimate Blend The Original Detox Drink Natural Tropical Ice Flavor 16 fl. by Zydot Unlimited, Inc. Reason: The ingredient list did not declare the preservatives (potassium sorbate, sodium benzoate) and food coloring (B1 and R40) in the product..

Details

Source

Food Recall

External ID

F-1272-2022

Action Date

2022-06-15

Status

Terminated

Category

food

Product Description

Zydot Ultimate Blend The Original Detox Drink Natural Tropical Ice Flavor 16 fl. oz. (473 ml) UPC packaged in plastic bottle with lid

Lot/Code Info: Lot #s 092921LT, 031422LT

Quantity Affected: 1150 bottles (total)

Reason for Recall

The ingredient list did not declare the preservatives (potassium sorbate, sodium benzoate) and food coloring (B1 and R40) in the product.

Distribution

USA

Type: Voluntary: Firm initiated

Recall Initiated: 2022-05-06

Company

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 197 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Zydot Unlimited, Inc has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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

How often does Zydot Unlimited, Inc have FDA actions?

Zydot Unlimited, Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1272-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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