Negita Cracker- Shrimp 2.8oz
Recalled by Hadson (Toko) Trading Co. Inc.
Food recall
Hadson (Toko) Trading Co. Inc.
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Hadson (Toko) Trading Co. Inc. has recalled Negita Cracker- Shrimp 2.8oz, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on May 6, 2026 and was initiated on April 16, 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 Negita Cracker- Shrimp 2.8oz, with approximately 142 units affected. The company behind the recall is Hadson (Toko) Trading Co. Inc., based in Maspeth, NY. The FDA describes the product as: “Negita Cracker- Shrimp 2.8oz”
Why was Negita Cracker- Shrimp 2.8oz recalled?
According to the FDA, the stated reason for the recall is: “Contains undeclared FD&C Yellow 6.” In plain terms, this recall relates to an undeclared ingredient or allergen.
An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.
What should you do?
If you think you may have bought Negita Cracker- Shrimp 2.8oz, compare it against the product description and identifying codes (UPC code: 4975934313310 Best by: 1/6/2027) 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 Hadson (Toko) Trading Co. Inc. or your local health authority.
About this recall
This recall was distributed in NY. 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
- May 6, 2026
- Recall started
- April 16, 2026
- Distributed in
- NY
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 Negita Cracker- Shrimp 2.8oz recalled?+
According to the FDA: Contains undeclared FD&C Yellow 6
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 Negita Cracker- Shrimp 2.8oz?+
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-0679-2026. Information last synced from the FDA on July 6, 2026.