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Lower risk Food recall · FDA · Published August 27, 2016

Westby 4% Cottage Cheese Recall: Phosphatase Residue Found

Westby Coop Creamery recalls 4% cottage cheese in 16oz, 22oz, and 24oz plastic containers due to phosphatase residue detected. Consumers should check lot codes and contact for details.

🇺🇸 FDA recall #F-0504-2017FoodWestby ›
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Recalling firmWestby Coop Creamery401 S Main St · Westby, WI 54667-1311
✎ GovInfoNow plain-language explainer

What happened, in plain English

Westby Coop Creamery is recalling 4% cottage cheese in 16-ounce, 22-ounce, and 24-ounce plastic containers because testing found phosphatase residue. This could pose a health risk if consumed, so affected consumers should stop using the product. Read more at govinfonow.com/recall/23393-westby-4-cottage-cheese-recall-phosphatase-residue-found.

Source Summary by GovInfoNow · govinfonow.com/recall/23393-westby-4-cottage-cheese-recall-phosphatase-residue-found · Updated October 9, 2026 · FDA enforcement record: FDA #F-0504-2017

Cite this page

“Westby 4% Cottage Cheese Recall: Phosphatase Residue Found.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23393-westby-4-cottage-cheese-recall-phosphatase-residue-found. Based on FDA recall #F-0504-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0504-2017%22&limit=1).

Why it’s dangerous

Phosphatase residue in the cottage cheese could cause health issues if consumed. The residue is a chemical that may affect digestion or cause allergic reactions in sensitive individuals.

Who’s affected

Consumers who purchased Westby, Food Club, Oberweis, or Shurfine brand 4% cottage cheese in 16oz, 22oz, or 24oz plastic containers. Those with the specific lot code 10-6-16 cc from Plant #55-372 are most at risk.

How to tell if you have this one

Check for 16-ounce, 22-ounce, or 24-ounce plastic containers labeled with Westby, Food Club, Oberweis, or Shurfine. Look for lot code 10-6-16 cc from Plant #55-372.

  • Brand
    Westby
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the lot code 10-6-16 cc on the container from Plant #55-372.

  2. Stop Using Product

    Discard the cottage cheese if it has the specific lot code and container size.

Where it went and when

Where it was distributed

Distributed in Illinois and Wisconsin.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: yesWIMichigan: not listedMINew York: not listedNYRhode 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: “WI, IL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois, Wisconsin.

Recall timeline

FDA terminated this recall 16 months after the firm started it.

1. Firm started the recall: Aug 27, 201612. FDA classified it Class II: Nov 23, 201623. Published in FDA’s Enforcement Report: Nov 30, 201634. FDA terminated the recall: Dec 28, 2017420162017
  1. Firm started the recall
  2. FDA classified it Class II
  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-0504-2017 (August 27, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0504-2017 to see it in context.
  • Plain-language summary written by qwen3:4b 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