FDA recall record

Ajinomoto Foods Item 5650173 Trader Joe's Japanese Style Fried Rice with recall — FDA H-0591-2026

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

Class IIclassification
H-0591-2026official record ID
Apr 1, 2026report date

Recall record at a glance

Official recordH-0591-2026
CategoryFood Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmAjinomoto Foods North America Inc.
Report dateApr 1, 2026
Recall initiation dateMar 3, 2026
Quantity3,059,808 lbs. or 127,492 cases (24 lbs. per case)
LocationOntario, CA, United States

Official product description

Item 5650173 Trader Joe's Japanese Style Fried Rice with Edamame, Tofu, and Hijiki Seaweed. SKU #097908. Net wt. 1lb. per bag. Retail bag UPC 00979085. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 24/1lb. bags per case. Case UPC 10097908500001. All products are intended to be stored frozen and fully cooked to 165F before eating.

Why the product was recalled

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

Distribution information

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.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.