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Use caution Food recall · FDA · Published April 16, 2026

Hadson Negita Cracker Recall: Undeclared FD&C Yellow 6

Hadson Trading recalls Negita Cracker- Shrimp 2.8oz due to undeclared FD&C Yellow 6. Check your UPC and best-by date for details.

🇺🇸 FDA recall #H-0679-2026FoodHadson (Toko) ›
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Contact the company

Recalling firmHadson (Toko) Trading Co. Inc.5718 Flushing Ave · Maspeth, NY 11378-3120
✎ GovInfoNow plain-language explainer

Hadson (Toko) Trading Co. Inc. is recalling Negita Cracker- Shrimp 2.8oz because it contains undeclared FD&C Yellow 6. This allergen information is missing from the label, which can be dangerous for individuals with specific sensitivities. The recall affects a small quantity of units distributed across several states. Read more at govinfonow.com/recall/6501-hadson-negita-cracker-recall-undeclared-fd-c-yellow-6.

Source Summary by GovInfoNow · govinfonow.com/recall/6501-hadson-negita-cracker-recall-undeclared-fd-c-yellow-6 · Updated October 9, 2026 · Official notice: FDA #H-0679-2026

Cite this page

“Hadson Negita Cracker Recall: Undeclared FD&C Yellow 6.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/6501-hadson-negita-cracker-recall-undeclared-fd-c-yellow-6. Based on FDA recall #H-0679-2026.

Hadson (Toko) Trading Co. Inc. voluntarily recalled Negita Cracker- Shrimp 2.8oz because it contains undeclared FD&C Yellow 6, the FDA said on April 16, 2026. The recall affects 142 units distributed in Connecticut, Georgia, Illinois, Massachusetts, Maryland, New Jersey, New York, Ohio, Pennsylvania, Texas, Utah, and Virginia.

How to tell if you have it

  • Brand: Hadson (Toko)
  • Product: Negita Cracker- Shrimp
  • Size: 2.8oz
  • UPC: 04975934313310
  • Best by date: 1/6/2027

The hazard

The product contains undeclared FD&C Yellow 6, which can cause allergic reactions in individuals sensitive to the dye. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show Hadson (Toko) Trading Co. Inc. has one other recall on record since October 14, 2020: an Eishindo Cup Jelly (Mini) choking hazard recall issued on that date. Other recent recalls of similar products include Rovira Tita Crackers Recall for undeclared FD&C colors (December 17, 2025), Rovira Snack Crackers Recall for undeclared FD&C colors (December 17, 2025), and Wont: Wonton Specialist Inc. Dumpling Skin Recall for undeclared Red 40 (July 28, 2026).

How to tell if you have this one

Check for Negita Cracker- Shrimp 2.8oz packages with UPC code 4975934313310 and a Best By date of 1/6/2027. The product was distributed in CT, GA, IL, MA, MD, NJ, NY, OH, PA, TX, UT, and VA.

  • Brand
    Hadson (Toko)
  • Product
    Negita Cracker- Shrimp 2.8oz
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product

    Verify if your package matches the UPC code 4975934313310 and Best By date 1/6/2027.

  2. Avoid Consumption

    Do not eat the product if it matches the recalled details due to the undeclared allergen.

Where it went and when

Where it was distributed

Distributed in 12 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: not listedCAUtah: yesUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “CT, GA, IL, MA, MD, NJ, NY, OH, PA, TX, UT, VA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Connecticut, Georgia, Illinois, Maryland, Massachusetts, New Jersey, New York, Ohio, Pennsylvania, Texas, Utah, Virginia.

Recall timeline

FDA published this recall 20 days after the firm started it.

1. Firm started the recall: Apr 16, 202612. FDA classified it Class II: Apr 28, 202623. Published in FDA’s Enforcement Report: May 6, 202632026
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-0679-2026 (April 16, 2026)
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA