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Class IIOngoing in FDA datasetRecall initiated Mar 3, 2026

Item 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct. Net wt. 8.92oz. per package. Retail…

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 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct. Net wt. 8.92oz. per package. Retail package UPC: 071757055483. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 20/8.92oz. packages or 11.15 lbs. per case. Carton UPC 10071757055480. All products are intended to be stored frozen and fully cooked to 165F before eating.
Package size8.92oz
UPC071757055483

FDA code information

Best By Dates: 10/13/2026 12/13/2026 3/7/2027

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 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct. Net wt. 8.92oz. per package. Retail package UPC: 071757055483. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 20/8.92oz. packages or 11.15 lbs. per case. Carton UPC 10071757055480. All products are intended to be stored frozen and fully cooked to 165F before eating.

Extracted codes and context

TypeCode / valueContext
UPC071757055483egetable Gyoza Dumplings 12ct. Net wt. 8.92oz. per package. Retail package UPC: 071757055483. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 20/8.92oz

Original FDA recall reason

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

Recall details

Recall number
H-0600-2026
Event ID
98535
FDA status
Ongoing
Initiated
Mar 3, 2026
Reported
Apr 1, 2026
Classified
Mar 20, 2026
Quantity
90,362 lbs. or 8,097 cases (11.15lb. per case)
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-0600-2026

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

Follow official FDA and manufacturer guidance.