RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) M…
Recalled by Raw Farm LLC
Food recall
Raw Farm LLC
Class I — most serious
There is a reasonable chance that using this product could cause serious health problems or death.
Raw Farm LLC has recalled RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) M…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on May 13, 2026 and was initiated on April 2, 2026. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) M…, with approximately Not provided affected. The company behind the recall is Raw Farm LLC, based in Fresno, CA. The FDA describes the product as: “RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) MADE WITH WHOLE RAW MILK MADE IN USA KEEP REFRIGERATED INGREDIENTS: whole raw milk, vegetable rennet, cultures, kosher sea salt Produced By: RAW FARM, LLC www.rawfarmusa.com 8 oz (227g) UPC: 83…”
Why was RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) M… recalled?
According to the FDA, the stated reason for the recall is: “Multi-state outbreak of E. coli O157:H7.” In plain terms, this recall relates to E. coli.
Escherichia coli (E. coli) is a large group of bacteria. While most types are harmless, certain strains such as O157:H7 can produce toxins that cause illness. Public health agencies note that symptoms can include severe stomach cramps, diarrhea, and vomiting, with young children and older adults facing a greater risk of complications.
What should you do?
If you think you may have bought RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) M…, compare it against the product description and identifying codes (8 oz - BATCH: 20260212, BEST BY: 5/13/2026 and all prior batches/dates. 16 oz - BATCH: 20251027-4, BEST BY: 8/23/2026 and all prior batches/dates.) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Raw Farm LLC or your local health authority.
About this recall
This recall was distributed in CA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Ongoing
- Date reported
- May 13, 2026
- Recall started
- April 2, 2026
- Distributed in
- CA
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) M… recalled?+
According to the FDA: Multi-state outbreak of E.
How serious is this recall?+
Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.
What should I do if I have RAW FARM RAW CHEDDAR Original NEVER WARMED ABOVE 102F (TRULY RAW) M…?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0762-2026. Information last synced from the FDA on July 5, 2026.