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Stop using now Food recall · FDA · Published February 16, 2024

Raw Farm Recalls Raw Cheddar Cheese Due to E. coli Risk

Raw Farm LLC recalls 8 oz blocks of raw cheddar cheese made from unpasteurized milk due to potential E. coli O157:H7 contamination.

🇺🇸 FDA recall #F-1373-2024FoodRaw Farm ›
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Recalling firmRaw Farm LLC7221 S Jameson Ave · Fresno, CA 93706-9386
✎ GovInfoNow plain-language explainer

Raw Farm LLC is recalling 8-ounce blocks of raw cheddar cheese made from unpasteurized milk because they may be contaminated with E. coli O157:H7. This is a Class I recall, indicating a serious health risk. The affected products were distributed to retailers and distribution centers in Texas, California, Colorado, and Arizona. Read more at govinfonow.com/recall/9580-raw-farm-recalls-raw-cheddar-cheese-due-to-e-coli.

Source Summary by GovInfoNow · govinfonow.com/recall/9580-raw-farm-recalls-raw-cheddar-cheese-due-to-e-coli · Updated October 9, 2026 · FDA enforcement record: FDA #F-1373-2024

Cite this page

“Raw Farm Recalls Raw Cheddar Cheese Due to E. coli Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/9580-raw-farm-recalls-raw-cheddar-cheese-due-to-e-coli. Based on FDA recall #F-1373-2024 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1373-2024%22&limit=1).

The FDA announced on Feb. 16, 2024, that Raw Farm LLC voluntarily recalled Raw Cheddar Cheese due to potential E. coli O157:H7 contamination. The recall affects 8 oz blocks distributed in Texas, California, Colorado, and Arizona.

How to tell if you have it

  • Brand: Raw Farm
  • Product: Raw Cheddar Cheese, made from unpasteurized milk, 8 oz (1/2 lb) block
  • UPC: 00835204001177
  • Batch: 20231113-1 or older

The hazard

The product poses a potential contamination risk with E. coli O157:H7. The FDA classified the recall as Class I, indicating a high probability of serious adverse health consequences.

Context

GovInfoNow's records show Raw Farm LLC has one other recall on record since April 2, 2026, involving shredded cheddar cheese and an E. coli outbreak risk. Other recent recalls of similar products include Twin Sisters Creamery Farmhouse Cheese Recall (Oct. 24, 2025), Twin Sisters Creamery Mustard Seed Cheese Recall (Oct. 24, 2025), and Boss Dairy Farms Mild Cheddar Cheese Recall (Nov. 16, 2025).

How to tell if you have this one

Check your refrigerator for 8-ounce blocks of Raw Cheddar Cheese made from unpasteurized milk that must be kept refrigerated under 40 degrees. Look for Item 1050, Barcode 835204001177, and Batch numbers 20231113 or older.

  • Brand
    Raw Farm
  • Product
    Raw Cheddar Cheese, made from unpasteurized milk, 8 oz (1/2 lb) block, Keep Refrigerated under 40 degrees
  • 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
    Products are distributed to retailers and distribution centers in the following U.S. states: TX, CA, CO, AZ. No foreign distribution.
Recall numberProduct, codes & lots
F-1372-2024Raw Cheddar Cheese, made from unpasteurized milk, 16 oz (1 lb) block, Keep Refrigerated under 40 degrees; Item 1075, Barcode 835204000156, Batch 20231113-1 or older
F-1373-2024Raw Cheddar Cheese, made from unpasteurized milk, 8 oz (1/2 lb) block, Keep Refrigerated under 40 degrees; Item 1050, Barcode 835204001177, Batch 20231113-1 or older
F-1374-2024Raw Cheddar Cheese, made from unpasteurized milk, 8 oz (1/2 lb), shredded, in a plastic bag, Keep Refrigerated under 40 degrees; Item 1080, Barcode 835204001184, Batch 20240116 or older
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the cheese

    Do not eat the recalled raw cheddar cheese blocks due to the risk of E. coli contamination.

  2. Discard or return the product

    Throw away the affected cheese or return it to the place of purchase for a refund, as no specific remedy details are provided in the record.

Where it went and when

Where it was distributed

Distributed in 4 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: 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: yesCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew 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: yesTXFlorida: not listedFL

FDA distribution: “Products are distributed to retailers and distribution centers in the following U.S. states: TX, CA, CO, AZ. No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California, Colorado, Texas.

Recall timeline

FDA terminated this recall 4 months after the firm started it.

1. Firm started the recall: Feb 16, 202412. FDA classified it Class I: Jun 17, 202423. FDA terminated the recall: Jun 25, 202434. Published in FDA’s Enforcement Report: Jun 26, 202442024
  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 #F-1373-2024 (February 16, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1373-2024 to see it in context.
  • 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