Class II Recall

Item 5650893 Ajinomoto Japanese-Style Vegetable Fried Rice made with hijiki seaweed, fried tofu, edamame, and other colo

Summary

The FDA issued a Class II for Item 5650893 Ajinomoto Japanese-Style Vegetable Fried Rice made with hijiki seaw by Ajinomoto Foods North America Inc.. Reason: Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide..

Details

Source

Food Recall

External ID

H-0594-2026

Action Date

2026-04-01

Status

Ongoing

Product Description

Item 5650893 Ajinomoto Japanese-Style Vegetable Fried Rice made with hijiki seaweed, fried tofu, edamame, and other colorful vegetables in an umami dashi sauce Net wt. 17oz. Retail box UPC 071757508934. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 8/17oz. boxes or 8.5 lbs. per case. Case UPC 10071757508931. All products are intended to be stored frozen and fully cooked to 165F before eating.

Lot/Code Info: Best By Date: 8/21/2026

Quantity Affected: 35,955 lbs. or 4,230 cases (8.5 lbs. case)

Reason for Recall

Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.

Distribution

Distributed in AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, and WY.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-03-03

Company

Ajinomoto Foods North America Inc.

Ontario, CA

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 64 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Ajinomoto Foods North America Inc. has 11 FDA actions in our database, including 11 recalls.

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 (Ajinomoto Foods North America Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Ajinomoto Foods North America Inc. have FDA actions?

Ajinomoto Foods North America Inc. has 11 FDA actions in our database, including 11 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0594-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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