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Use caution Food recall · FDA · Published October 6, 2017

Cooperstown Cheese Toma Celena Cheese Recall: Listeria Contamination Risk

Cooperstown Cheese Company recalls Toma Celena cheese due to potential Listeria monocytogenes contamination. Affected lots 51017 and 52417 from plant 36-8524. Consumers should avoid these products.

🇺🇸 FDA recall #F-0139-2018FoodCooperstown Cheese Company ›
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Recalling firmCooperstown Cheese Company, LLC107 Oxbow Rd · Milford, NY 13807-1131
✎ GovInfoNow plain-language explainer

What happened, in plain English

Cooperstown Cheese Company is recalling Toma Cel:ena cheese because it may be contaminated with Listeria monocytogenes. This bacteria can cause serious illness, especially in pregnant women, newborns, and the elderly. The recall affects specific lots from a single production plant. Read more at govinfonow.com/recall/20381-cooperstown-cheese-toma-celena-cheese-recall-listeria-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/20381-cooperstown-cheese-toma-celena-cheese-recall-listeria-contamination-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0139-2018

Cite this page

“Cooperstown Cheese Toma Celena Cheese Recall: Listeria Contamination Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20381-cooperstown-cheese-toma-celena-cheese-recall-listeria-contamination-risk. Based on FDA recall #F-0139-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0139-2018%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacterium that can cause severe infections, particularly in vulnerable groups like pregnant women, newborns, and the elderly. Contaminated cheese can lead to foodborne illness if consumed.

Who’s affected

Anyone who purchased Toma Celena cheese from Cooperstown Cheese Company's plant with lot numbers 51017 or 52417. Pregnant individuals, newborns, and the elderly are at higher risk for serious illness from Listeria.

How to tell if you have this one

Check the package for lot numbers 51017 or 52417. The product was made at plant number 36-8524. All package sizes are affected.

  • Brand
    Cooperstown Cheese Company
  • Category
    Food
FDA recall event · 3 products

All 3 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Terminated
  • Distribution
    NY
Recall numberProduct, codes & lotsQuantity
F-0139-2018Toma Celena, A nutty, complex, alpine table cheese. All package sizes are subject to the recall and the plant number on the label is 36-8524.; lot 51017 and 5241753 wheels
F-0140-2018Roasted Garlic Cheddar, Raw milk. All package sizes are subject to the recall and the plant number on the label is 36-8524.; Lot 52417 and 6071723 wheels
F-0141-2018Roasted Garlic and Black Peppercorns. All package sizes are subject to the recall and the plant number on the label is 36-8524.; Lot 524177 wheels
Based on the official FDA remedy

What to do — step by step

  1. Check Package Details

    Look for lot numbers 51017 or 52417 on the label to identify affected products.

Where it went and when

Where it was distributed

Distributed in New York.

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: 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: “NY” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: New York.

Recall timeline

FDA terminated this recall 45 days after the firm started it.

1. Firm started the recall: Oct 6, 201712. FDA classified it Class I: Nov 8, 201723. Published in FDA’s Enforcement Report: Nov 8, 201734. FDA terminated the recall: Nov 20, 201742017
  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-0139-2018 (October 6, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0139-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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