CLASS II Food recall · Reported 12 Nov 2025 · FDA Enforcement Report

Frozen Coconut bar recalled by Que Rikura's Products

Que Rikura's Products is recalling Frozen Coconut bar, distributed in Florida. The recall was initiated on 3 Oct 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code: 392505 Expiration Date:03/26/2027
Quantity recalled31,953 cases Coconut 4oz bars

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0152-2026
FDA event ID
97761
Recalling firm
Que Rikura's Products, Hialeah, FL
Classification
Class II
Status
Terminated
Recall initiated
3 Oct 2025
FDA classified
3 Nov 2025
Reported
12 Nov 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Sulfites
Product category
Other

Timeline

3 Oct 2025Recall initiated by company
3 Nov 2025Classified by FDA+31 days
12 Nov 2025Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared sulfites in product label.

Product as listed by the FDA

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

Where it was distributed

Florida

Florida

Questions about this recall

Why was it recalled?

Undeclared sulfites in product label.

Which lots are affected?

Lot Code: 392505 Expiration Date:03/26/2027

Where was it sold?

Florida

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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