RecallHawk
Class I Recall

RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204001160

Raw Farm LLC

Summary

The FDA issued a Class I for RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204001160 by Raw Farm LLC. Reason: Multi-state outbreak of E. coli O157:H7..

Details

Source

Food Recall

External ID

H-0766-2026

Action Date

2026-05-13

Status

Ongoing

Category

food

Product Description

RAW FARM ORIGINAL RAW CHEDDAR 80 OZ [BULK ITEM] UPC: 835204001160

Lot/Code Info: 80 oz - BATCH: 20251015-4, BEST BY: 8/11/2026 and all prior batches/dates.

Quantity Affected: Not provided

Reason for Recall

Multi-state outbreak of E. coli O157:H7.

Distribution

U.S. distribution: AZ, CA, CO, FL, GA, IL, IN, MD, NV, TX. Foreign distribution: None.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-04-02

Company

Raw Farm LLC

Fresno, CA

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 93 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Raw Farm LLC has 8 FDA actions in our database, including 8 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Raw Farm LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Raw Farm LLC have FDA actions?

Raw Farm LLC has 8 FDA actions in our database, including 8 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0766-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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