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