RecallHawk
Class II Recall

Mai California Roll WR - UPC 840031402639 5.9 oz (167g) Plastic tray with plastic lid

HANA GROUP

Summary

The FDA issued a Class II for Mai California Roll WR - UPC 840031402639 5.9 oz (167g) Plastic tray with plast by HANA GROUP. Reason: Wheat and Soy missing allergens from the product Contains Statement..

Details

Source

Food Recall

External ID

H-0209-2026

Action Date

2025-11-19

Status

Terminated

Category

food

Product Description

Mai California Roll WR - UPC 840031402639 5.9 oz (167g) Plastic tray with plastic lid

Lot/Code Info: Handcrafted daily: 10/30/2025, Best By: 10/31/2025 Handcrafted daily: 10/31/2025, Best By: 11/01/2025

Quantity Affected: 373 packages

Reason for Recall

Wheat and Soy missing allergens from the product Contains Statement.

Distribution

(FL, VA, IL, NE, MN, IN, LA, OK) - retail kiosks

Type: Voluntary: Firm initiated

Recall Initiated: 2025-10-31

Company

HANA GROUP

Irving, TX

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 44 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 (HANA GROUP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does HANA GROUP have FDA actions?

This is the only FDA action we have on record for HANA GROUP in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0209-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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