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Lower risk Food recall · FDA · Published January 3, 2020

Ducktrap River Herring in Wine Sauce Recall: Undeclared Milk Hazard

Ducktrap River of Maine recalls 12 oz. Herring Center Cuts in Wine Sauce (sold by Jul 29, 2020) due to undeclared milk. Consumers should check UPC 082674072408 for affected products.

🇺🇸 FDA recall #F-0633-2020FoodDucktrap River of Maine ›
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Contact the company

Recalling firmDucktrap River of Maine LLC57 Little River Dr · Belfast, ME 04915-6035
✎ GovInfoNow plain-language explainer

What happened, in plain English

Ducktrap River of Maine is recalling 12-ounce herring center cuts in wine sauce because it contains undeclared milk. This could cause allergic reactions for people with milk allergies. The recall affects products sold by July 29, 2020. Read more at govinfonow.com/recall/16069-ducktrap-river-herring-in-wine-sauce-recall-undeclared-milk-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/16069-ducktrap-river-herring-in-wine-sauce-recall-undeclared-milk-hazard · Updated October 5, 2026 · FDA enforcement record: FDA #F-0633-2020

Cite this page

“Ducktrap River Herring in Wine Sauce Recall: Undeclared Milk Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16069-ducktrap-river-herring-in-wine-sauce-recall-undeclared-milk-hazard. Based on FDA recall #F-0633-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0633-2020%22&limit=1).

Why it’s dangerous

The herring sauce contains milk that wasn't listed on the label. This poses a risk for individuals with milk allergies who might react to the hidden milk ingredient.

Who’s affected

People who purchased the recalled herring in wine sauce from stores selling it by July 29, 2020. Those with milk allergies are at higher risk of allergic reactions.

How to tell if you have this one

Check for the product name 'Herring Center Cuts in Wine Sauce', 12 oz. size, and UPC 082674072408. Products sold by July 29, 2020 are affected.

  • Brand
    Ducktrap River of Maine
  • Product
    Ducktrap River of Maine Herring Center Cuts in Wine Sauce, 12 oz
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC 082674072408 on the packaging to confirm if your product is recalled.

Where it went and when

Where it was distributed

Distributed in 14 states.

Alaska: not listedAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: yesLAMississippi: not listedMSAlabama: yesALGeorgia: yesGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “AL, GA, LA, ME, MA, MO, NH, NY, NC, OH, SC, TN, VT, VA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Georgia, Louisiana, Maine, Massachusetts, Missouri, New Hampshire, New York, North Carolina, Ohio, South Carolina, Tennessee, Vermont, Virginia.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Jan 3, 202012. FDA classified it Class I: Feb 4, 202023. Published in FDA’s Enforcement Report: Feb 12, 202034. FDA terminated the recall: Mar 30, 202042020
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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 #F-0633-2020 (January 3, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0633-2020 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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