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HANA GROUP Recall: Wheat and Soy missing allergens from the product Contains Statement.

United States

TerminatedClass II

Company
HANA GROUP
Product
Mai California Roll WR - UPC 840031402639 5.9 oz (167g) Pla…
Recall date
October 31, 2025
Terminated
February 25, 2026
Source
FDA

Reason for recall

Wheat and Soy missing allergens from the product Contains Statement.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Mai California Roll WR - UPC 840031402639 5.9 oz (167g) Plastic tray with plastic lid 840031402639 373 packages Handcrafted daily: 10/30/2025, Best By: 10/31/2025 Handcrafted daily: 10/31/2025, Best By: 11/01/2025

Distribution

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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-0209-2026
Event ID
97943
Status
Terminated
Classification
Class II
Company
HANA GROUP
Product description
Mai California Roll WR - UPC 840031402639 5.9 oz (167g) Plastic tray with plastic lid
Quantity
373 packages
Reason
Wheat and Soy missing allergens from the product Contains Statement.
Recall initiation date
October 31, 2025
Report date
November 19, 2025
Classification date
Not published in this source record
Termination date
February 25, 2026
Distribution pattern
(FL, VA, IL, NE, MN, IN, LA, OK) - retail kiosks
UPC, lot, and code information
UPC 840031402639; Handcrafted daily: 10/30/2025, Best By: 10/31/2025 Handcrafted daily: 10/31/2025, Best By: 11/01/2025
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: HANA GROUP

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Florida 1
Virginia 1
Illinois 1
Nebraska 1
Minnesota 1
Indiana 1
Louisiana 1
Oklahoma 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

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.

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