Calypso Tropic Tango Lemonade. 16 FL oz (1PT) (473 ML). UPC 0 79581-18709 7. Keep Refrigerated After Opening. King J
Summary
The FDA issued a Class II for Calypso Tropic Tango Lemonade. 16 FL oz (1PT) (473 ML). UPC 0 79581-18709 7. by King Juice Company, Inc.. Reason: Product contains undeclared Yellow No. 5..
Details
Source
Food Recall
External ID
H-0685-2026
Action Date
2026-05-06
Status
Ongoing
Category
food
Product Description
Calypso Tropic Tango Lemonade. 16 FL oz (1PT) (473 ML). UPC 0 79581-18709 7. Keep Refrigerated After Opening. King Juice Company, Inc., Milwaukee, Wisconsin 53221.
Lot/Code Info: All Lot Codes including and prior to 01APR2027
Quantity Affected: 299,779 cases (12 bottles per case)
Reason for Recall
Product contains undeclared Yellow No. 5.
Distribution
Nationwide. Outside the US to Australia, New Zealand, Singapore, and Trinidad and Tobago
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-23
Company
Milwaukee, WI
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 19 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 (King Juice Company, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does King Juice Company, Inc. have FDA actions?
This is the only FDA action we have on record for King Juice Company, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0685-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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