Frozen Coconut bar Net wt. 4oz (113g) single bars packed in a plastic cup. UPC: 61058590845. Crafted by Fruitique Intern
Summary
The FDA issued a Class II for Frozen Coconut bar Net wt. 4oz (113g) single bars packed in a plastic cup. UPC: by QUE RIKURA'S PRODUCTS, CORP. Reason: Undeclared sulfites in product label..
Details
Source
Food Recall
External ID
H-0152-2026
Action Date
2025-11-12
Status
Terminated
Category
food
Product Description
Frozen Coconut bar Net wt. 4oz (113g) single bars packed in a plastic cup. UPC: 61058590845. Crafted by Fruitique International Miami USA 33016. Phone 1(888)960-6024
Lot/Code Info: Lot Code: 392505 Expiration Date:03/26/2027
Quantity Affected: 31,953 cases Coconut 4oz bars
Reason for Recall
Undeclared sulfites in product label.
Distribution
Florida
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-03
Company
Hialeah, FL
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 34 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 (QUE RIKURA'S PRODUCTS, CORP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does QUE RIKURA'S PRODUCTS, CORP have FDA actions?
This is the only FDA action we have on record for QUE RIKURA'S PRODUCTS, CORP in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0152-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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