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Class IIOngoing in FDA datasetRecall initiated Mar 3, 2026

Item 81097 Ajinomoto Ling Ling Restaurant Style Fried Rice Savory Vegetable - A Chinese Style…

Recalling firm: Ajinomoto Foods North America Inc.

Why it was recalled

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

Check your package

Compare the exact product and package details with the label you have.

ProductItem 81097 Ajinomoto Ling Ling Restaurant Style Fried Rice Savory Vegetable - A Chinese Style Fried Rice with Edamame, Carrots, Fire Roasted Corn & Red Bell Peppers Prepared with Sweet Soy Sauce Infused Rice. Net wt. 17oz. Retail box UPC 010878810915. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 6/17oz. boxes per case. Case UPC 10010878810912. All products are intended to be stored frozen and fully cooked to 165F before eating.
Package size17oz
UPC010878810915

FDA code information

Best By Dates: 9/21/2026 3/8/2027

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Item 81097 Ajinomoto Ling Ling Restaurant Style Fried Rice Savory Vegetable - A Chinese Style Fried Rice with Edamame, Carrots, Fire Roasted Corn & Red Bell Peppers Prepared with Sweet Soy Sauce Infused Rice. Net wt. 17oz. Retail box UPC 010878810915. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 6/17oz. boxes per case. Case UPC 10010878810912. All products are intended to be stored frozen and fully cooked to 165F before eating.

Extracted codes and context

TypeCode / valueContext
UPC010878810915eppers Prepared with Sweet Soy Sauce Infused Rice. Net wt. 17oz. Retail box UPC 010878810915. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 6/17oz. b

Original FDA recall reason

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

Recall details

Recall number
H-0596-2026
Event ID
98535
FDA status
Ongoing
Initiated
Mar 3, 2026
Reported
Apr 1, 2026
Classified
Mar 20, 2026
Quantity
24,796 lbs. or 3,780 cases
Location
Ontario, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

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.

FDA source record · H-0596-2026

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.