FDA recall record

Ajinomoto Foods Item 81153 Kroger Chinese Inspiration Vegetable Fried Rice recall — FDA H-0598-2026

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

Class IIclassification
H-0598-2026official record ID
Apr 1, 2026report date

Recall record at a glance

Official recordH-0598-2026
CategoryFood Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmAjinomoto Foods North America Inc.
Report dateApr 1, 2026
Recall initiation dateMar 3, 2026
Quantity905,363 lbs. or 109,741 cases (8.25 lbs. per case)
LocationOntario, CA, United States

Official product description

Item 81153 Kroger Chinese Inspiration Vegetable Fried Rice - Blend of long grain rice assorted vegetables & egg. Net wt. 22oz. Retail box UPC 011110041623. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 6/22oz. boxes or 8.25 lbs. per case. Case UPC 10011110041620. 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

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