H-0593-2026Class II

Ajinomoto Foods North America Inc.

Recalling firm

Product type

Food / supplement / cosmetic

Status

Ongoing

Report date

2026-04-01

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.

Firm state

Product quantity

3,862,944 lbs. or 143,072 cases (27 lbs. per case)

Initiated by

Voluntary: Firm initiated

SPEQ quality domain

Environmental Monitoring

Reason for recall

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

Product description

Item 5650883 Ajinomoto Teppanyaki Style Vegetable Fried Rice - Japanese-style fried rice made with colorful vegetables in an aromatic garlic butter sauce. There are 6/9oz. bags per box or 54oz per box. Retail box UPC 071757508835. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 8/54oz boxes or 27lb. per case. Case UPC 10071757508832. All products are intended to be stored frozen and fully cooked to 165F before eating.

Code / lot info

Best If Use By Dates Range: 5/21/2026 to 05/05/2027 Best If Use By Dates: 5/21/2026 5/22/2026 5/25/2026 6/3/2026 6/4/2026 6/5/2026 6/6/2026 6/11/2026 6/12/2026 6/13/2026 6/16/2026 6/17/2026 7/2/2026 7/3/2026 7/6/2026 7/7/2026 7/8/2026 7/9/2026 7/21/2026 8/5/2026 8/6/2026 8/10/2026 8/11/2026 8/18/2026 8/19/2026 8/20/2026 8/24/2026 8/25/2026 8/26/2026 9/3/2026 9/4/2026 9/5/2026 9/6/2026 9/10/2026 9/11/2026 9/12/2026 9/13/2026 9/18/2026 9/20/2026 9/24/2026 10/1/2026 10/23/2026 10/24/2026 10/28/2026 11/7/2026 11/8/2026 11/13/2026 12/12/2026 12/13/2026 12/20/2026 1/23/2027 1/24/2027 1/25/2027 2/19/2027 2/21/2027 2/22/2027 2/27/2027 2/28/2027 3/5/2027 3/12/2027 3/25/2027 3/26/2027 4/10/2027 4/30/2027 5/5/2027

Other recalls SPEQ maps to Environmental Monitoring

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See all Environmental Monitoring recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.