Item 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct. Net wt. 8.92oz. per package. Retail package UPC: 071757055483. P
Summary
The FDA issued a Class II for Item 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct. Net wt. 8.92oz. per packa by Ajinomoto Foods North America Inc.. Reason: Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide..
Details
Source
Food Recall
External ID
H-0600-2026
Action Date
2026-04-01
Status
Ongoing
Category
food
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.
Lot/Code Info: Best By Dates: 10/13/2026 12/13/2026 3/7/2027
Quantity Affected: 90,362 lbs. or 8,097 cases (11.15lb. per case)
Reason for Recall
Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-03-03
Company
Ontario, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 64 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Ajinomoto Foods North America Inc. has 11 FDA actions in our database, including 11 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Ajinomoto Foods North America Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ajinomoto Foods North America Inc. have FDA actions?
Ajinomoto Foods North America Inc. has 11 FDA actions in our database, including 11 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0600-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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