J F C International Futaba Sesame Hijiki Rice Seasoning Recall

Why it was recalled

Firm discovered that seasoning product imported from Japan lacks an English language label and does not declare Wheat, Soybean and Fish (Bonito) allergens.

Product description

Futaba Sesame Hijiki Rice Seasoning; 2.29 oz. glass jar; 4 902533 023173

Lot numbers, UPCs & expiration codes

All lots distributed between June 19, 2016 and June 19, 2017.

Where it was sold

WA, OR, TX, CA, UT, NV, AZ, NY, MA, CT, CO, WV, MD, VA, NC, MD, PA..

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-2595-2017
Classification: Class I
Status: Terminated
Recall initiated: Jun 20, 2017
FDA report date: Jul 26, 2017
Quantity: 36 cases, 30 x 2.29 oz.bottles per case
Recall type: Voluntary: Firm initiated
Recalling firm: J F C International Inc

Original FDA data

Every field from FDA enforcement report F-2595-2017, exactly as published.

Show all FDA fields

City: Commerce
State: CA
Status: Terminated
Country: United States
Event ID: 77597
Address: 7101 E Slauson Ave
Code information: All lots distributed between June 19, 2016 and June 19, 2017.
Postal code: 90040-3622
Report date: Jul 26, 2017
Product type: Food
Recall number: F-2595-2017
Classification: Class I
Recalling firm: J F C International Inc
Product quantity: 36 cases, 30 x 2.29 oz.bottles per case
Termination date: Sep 11, 2017
Reason for recall: Firm discovered that seasoning product imported from Japan lacks an English language label and does not declare Wheat, Soybean and Fish (Bonito) allergens.
Voluntary / mandated: Voluntary: Firm initiated
Product description: Futaba Sesame Hijiki Rice Seasoning; 2.29 oz. glass jar; 4 902533 023173
Distribution pattern: WA, OR, TX, CA, UT, NV, AZ, NY, MA, CT, CO, WV, MD, VA, NC, MD, PA..
Recall initiation date: Jun 20, 2017
Initial firm notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date: Jul 14, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2595-2017, published Jul 26, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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