Coconut Drink 1; NET VOLUME: 1L; Ingredients: Coconut water, freshly squeezed coconut gravy, white granulated sugar, emu
Summary
The FDA issued a Class II for Coconut Drink 1; NET VOLUME: 1L; Ingredients: Coconut water, freshly squeezed co by HEYTEA USA INC. Reason: Product contains undeclared milk..
Details
Source
Food Recall
External ID
H-0646-2026
Action Date
2026-04-08
Status
Ongoing
Category
food
Product Description
Coconut Drink 1; NET VOLUME: 1L; Ingredients: Coconut water, freshly squeezed coconut gravy, white granulated sugar, emulsion stabilizer [sodium caseinate, mono- and diglycerides fatty acid esters, sucrose fatty acid esters]; Storage Condition: Room temperature; Manufactured in: Hainan, China; imported By: HK HEYTEA FOOD AND BEVERAGE MANAGEMENT LIMITED; For catering establishment; UPC: 673367992785
Lot/Code Info: Batch Numbers: 2025/03/25 2025/04/06 2025/04/12 2025/08/17 2025/09/04 2025/09/08 2025/09/18
Quantity Affected: 12677 cartons
Reason for Recall
Product contains undeclared milk.
Distribution
New York, New Jersey, Massachusetts, Virginia, Maryland, California, Washington, Texas
Type: Voluntary: Firm initiated
Recall Initiated: 2026-03-30
Company
Santa Ana, 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 59 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 (HEYTEA USA INC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does HEYTEA USA INC have FDA actions?
This is the only FDA action we have on record for HEYTEA USA INC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0646-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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