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Lower risk Food recall · FDA · Published November 7, 2025

Anthony's BBQ Sauce Recall: Undeclared Fish Allergen in 15oz Bottle

Anthony's BBQ recalls 15oz glass bottles of Barbecue & Dip-It Sauce due to undeclared fish allergen from Worcestershire sauce. Consumers should check UPC 689076622721 for affected products.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-0407-2026FoodAnthony's BBQ ›
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Contact the company

Recalling firmAnthony's BBQ97990 W Benham Ln · Harbor, OR 97415
✎ GovInfoNow plain-language explainer

Anthony's BBQ is recalling 15-ounce glass bottles of Barbecue & Dip-It Sauce because they contain an undeclared fish allergen from Worcestershire sauce. This poses a risk for people with fish allergies who might consume the product without knowing. Read more at govinfonow.com/recall/6993-anthony-s-bbq-sauce-recall-undeclared-fish-allergen-in-15oz.

Source Summary by GovInfoNow · govinfonow.com/recall/6993-anthony-s-bbq-sauce-recall-undeclared-fish-allergen-in-15oz · Updated August 17, 2026 · Official notice: FDA #H-0407-2026

Cite this page

“Anthony's BBQ Sauce Recall: Undeclared Fish Allergen in 15oz Bottle.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/6993-anthony-s-bbq-sauce-recall-undeclared-fish-allergen-in-15oz. Based on FDA recall #H-0407-2026.

The FDA announced on Nov. 7, 2025, that Anthony's BBQ voluntarily recalled its Barbecue & Dip-It Sauce due to an undeclared fish allergen. The agency said the product poses a risk to consumers with fish allergies.

How to tell if you have it

  • Anthony's Barbecue & Dip-It Sauce
  • 15 oz. (425g) glass bottle
  • UPC 6 89076 62272 1

The hazard

The FDA said the label does not declare Worcestershire sauce, which contains anchovy. This undeclared allergen can cause serious allergic reactions in sensitive individuals.

Context

GovInfoNow's records show other recent recalls of similar products include Booey's Dragon's Breath Sauce Recall (2026-03-23), Savannah Bee Company Honey BBQ Sauce Mustard Recall (2026-02-27), and Pack'n Fresh Hondashi Seasoning Recall (2026-07-09).

How to tell if you have this one

Check for the 15-ounce glass bottle with UPC 689076622721. The product name is Anthony's Barbecue & Dip-It Sauce.

  • Brand
    Anthony's BBQ
  • Product
    Anthony's Barbecue & Dip-It Sauce, 15 oz. (425g) glass bottle, UPC 6 89076 62272 1. Anthony's BBQ Sauce PO Box 3239
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the UPC 689076622721 on the bottle to confirm if it's affected.

Where it went and when

Where it was distributed

Distributed in Oregon.

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: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: 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: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Distributed only in OR.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Oregon.

Recall timeline

FDA terminated this recall 2 months after the firm started it.

1. Firm started the recall: Nov 7, 202512. FDA classified it Class I: Jan 16, 202623. FDA terminated the recall: Jan 21, 202634. Published in FDA’s Enforcement Report: Jan 28, 2026420252026
  1. Firm started the recall
  2. FDA classified it Class I
  3. FDA terminated the recall
  4. 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-0407-2026 (November 7, 2025)
  • Plain-language summary written by qwen3:4b on August 17, 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