Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumplings 12…
Recalled by Ajinomoto Foods North America Inc.
Food recall
Ajinomoto Foods North America Inc.
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Ajinomoto Foods North America Inc. has recalled Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumplings 12…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on April 1, 2026 and was initiated on March 3, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumplings 12…, with approximately 537,033 lbs. or 53,436 cases (20/12ct. bags per case) affected. The company behind the recall is Ajinomoto Foods North America Inc., based in Ontario, CA. The FDA describes the product as: “Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumplings 12ct. Retail bag UPC: None. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 20/12ct. bags per case. Case UPC 10071757080246. All produ…”
Why was Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumplings 12… recalled?
According to the FDA, the stated reason for the recall is: “Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.” In plain terms, this recall relates to foreign material.
A foreign material recall means that pieces of something which should not be in food — such as metal, plastic, or glass — may be present. These can pose a choking hazard or cause injury. Recalls like these are issued to remove the affected product before anyone is hurt.
What should you do?
If you think you may have bought Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumplings 12…, compare it against the product description and identifying codes (Best If Use By Dates Range: 06/19/2026 to 04/10/2027 Best By Dates: 6/19/2026 6/20/2026 7/17/2026 7/28/2026 8/6/2026 8/7/2026 9/18/2026 10/24/2026 11/7/2026 11…) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Ajinomoto Foods North America Inc. or your local health authority.
About this recall
This recall was distributed in CA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Ongoing
- Date reported
- April 1, 2026
- Recall started
- March 3, 2026
- Distributed in
- CA
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumplings 12… recalled?+
According to the FDA: Foreign objects are glass varying in size from 1-3cm long and 2-4mm wide.
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumplings 12…?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0599-2026. Information last synced from the FDA on July 6, 2026.