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Use caution Food recall · FDA · Published May 28, 2026

Wise Foods Recalls Onion Rings Due to Undeclared Allergens

Wise Foods is recalling 3.75 oz Onion Rings due to undeclared Yellow 5, 6, Blue 1, and unapproved Red 3 dyes. Check your lot codes.

🇺🇸 FDA recall #H-1146-2026FoodWise Foods ›
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Recalling firmWise Foods Inc228 Rasely St · Berwick, PA 18603-4533
✎ GovInfoNow plain-language explainer

What happened, in plain English

Wise Foods Inc has recalled 490 cases of its 3.75 oz Wise Onion Rings because the product contains undeclared food colorings (Yellow 5, Yellow 6, Blue 1) and an unapproved dye (Red 3). These ingredients are not listed on the label, which poses a risk to consumers with allergies or sensitivities to these substances. The recall covers specific lots distributed in North Carolina, Virginia, Pennsylvania, New Jersey, New York, South Carolina, and Florida. Read more at govinfonow.com/recall/6196-wise-foods-recalls-onion-rings-due-to-undeclared-allergens.

Source Summary by GovInfoNow · govinfonow.com/recall/6196-wise-foods-recalls-onion-rings-due-to-undeclared-allergens · Updated October 9, 2026 · Official notice: FDA #H-1146-2026

Cite this page

“Wise Foods Recalls Onion Rings Due to Undeclared Allergens.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/6196-wise-foods-recalls-onion-rings-due-to-undeclared-allergens. Based on FDA recall #H-1146-2026.

Why it’s dangerous

The product contains undeclared food colorings and an unapproved dye that are not listed on the packaging. This creates a risk for individuals with allergies or sensitivities to these specific substances, as they may unknowingly ingest them.

Who’s affected

Consumers who purchased the recalled Wise Onion Rings from the affected states are at risk if they have allergies or sensitivities to Yellow 5, Yellow 6, Blue 1, or Red 3. Individuals who do not consume these specific dyes are not affected by this recall.

How to tell if you have this one

Check your package for the brand 'Wise Foods' and product name 'Onion Rings', 3.75 oz size, packaged in metalized film inside cardboard cartons. Look for UPC 041262288874 and one of the following lot codes (expiration dates): AUG0326, AUG1026, or AUG1726.

  • Brand
    Wise Foods
  • Product
    Wise Onion Rings, 3.75 oz, metalized film in cardboard cartons, 14 bags per case
  • Category
    Food

Where it went and when

Where it was distributed

Distributed in 7 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “The adulterated product was distributed to the following States: NC, VA, PA, NJ, NY, SC, FL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, Virginia.

Recall timeline

FDA published this recall 48 days after the firm started it.

1. Firm started the recall: May 28, 202612. FDA classified it Class II: Jul 7, 202623. Published in FDA’s Enforcement Report: Jul 15, 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-1146-2026 (May 28, 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