H-0592-2026Class 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

9,885,240 lbs. or 411,885 cases (24 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 5650233 Trader Joe's Vegetable Fried Rice, net wt. 1lb per bag. Retail bag UPC 00521482. 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 10052148200001. All products are intended to be stored frozen and fully cooked to 165F before eating.

Code / lot info

Best By Dates Range: 2/28/2026 to 11/19/2026 Best By Dates: 2/28/2026 3/3/2026 3/4/2026 3/8/2026 3/10/2026 3/17/2026 3/18/2026 3/20/2026 3/22/2026 3/25/2026 3/31/2026 4/1/2026 4/2/2026 4/9/2026 4/10/2026 4/11/2026 4/12/2026 4/23/2026 4/24/2026 4/28/2026 4/29/2026 4/30/2026 5/3/2026 5/8/2026 5/12/2026 5/13/2026 5/14/2026 5/16/2026 5/21/2026 5/22/2026 5/27/2026 5/28/2026 5/29/2026 5/31/2026 6/4/2026 6/14/2026 6/19/2026 6/20/2026 6/26/2026 6/27/2026 7/7/2026 7/10/2026 7/11/2026 7/14/2026 7/21/2026 7/26/2026 7/28/2026 7/30/2026 7/31/2026 8/7/2026 8/8/2026 8/11/2026 8/12/2026 8/18/2026 8/19/2026 8/20/2026 8/21/2026 8/25/2026 8/26/2026 9/2/2026 9/3/2026 9/10/2026 9/11/2026 9/15/2026 9/16/2026 9/17/2026 9/24/2026 9/25/2026 9/29/2026 10/2/2026 10/6/2026 10/7/2026 10/13/2026 10/14/2026 10/18/2026 10/22/2026 10/23/2026 10/25/2026 10/27/2026 11/5/2026 11/6/2026 11/8/2026 11/19/2026

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.