King Juice Company, Inc. Recall: Product contains undeclared Yellow No. 5.
United States
TerminatedClass II
- Company
- King Juice Company, Inc.
- Product
- Calypso Tropic Tango Lemonade. 16 FL oz (1PT) (473 ML). UP…
- Recall date
- April 23, 2026
- Terminated
- July 10, 2026
- Source
- FDA
Reason for recall
Product contains undeclared Yellow No. 5.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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. | Not published in this source record | 299,779 cases (12 bottles per case) | All Lot Codes including and prior to 01APR2027 |
Distribution
- Nationwide. Outside the US to Australia
- New Zealand
- Singapore
- and Trinidad and Tobago
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0685-2026
- Event ID
- 98808
- Status
- Terminated
- Classification
- Class II
- Company
- King Juice Company, Inc.
- 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.
- Quantity
- 299,779 cases (12 bottles per case)
- Reason
- Product contains undeclared Yellow No. 5.
- Recall initiation date
- April 23, 2026
- Report date
- May 6, 2026
- Classification date
- Not published in this source record
- Termination date
- July 10, 2026
- Distribution pattern
- Nationwide. Outside the US to Australia, New Zealand, Singapore, and Trinidad and Tobago
- UPC, lot, and code information
- All Lot Codes including and prior to 01APR2027
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: King Juice Company, Inc.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
