Raw Farm LLC Recall History
Raw Farm LLC has had 1 FDA-tracked food recall since 2026, including 1 Class I recall (most serious). The full list below — sourced from the FDA openFDA enforcement database — shows dates, products, reasons, and classifications for every recall on record.
Key Facts
- Total Recalls
- 1
- Years in FDA Data
- Since 2026
- Class I (Most Serious)
- 1
- Most Common Reason
- E. coli contamination (1)
- Latest Recall
- Apr 2, 2026
- First Recorded Recall
- Apr 2, 2026
- States Affected
- AZ, CA, CO, FL, GA, IL, IN, MD, NV, TX
- Currently Active
- 1
- Data Source
- FDA openFDA + USDA FSIS
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Complete Recall List (1 Records)
Every Raw Farm LLC recall in the FDA enforcement database, newest first. Each row links to the full recall notice with affected product codes, distribution, and consumer guidance.
| Date | Product | Class | Status |
|---|---|---|---|
| Apr 2, 2026 | RAW FARM RAW CHEDDAR SIMPLY SHREDDED Original MADE WITH: ... | Class I | Active |
Recall data sourced from the FDA's recalls and safety alerts database. Class I recalls indicate a reasonable probability of serious adverse health consequences. Always check the USDA FSIS recall list for meat and poultry products.
Frequently Asked Questions
Yes, Raw Farm LLC has 1 FDA food recall on record, including 1 Class I (dangerous) recall. There is currently 1 active recall.
Raw Farm LLC currently has 1 active recall. Check the recall details above to see if your specific product is affected. If you have a recalled product, do not consume it.
Raw Farm LLC's 1 recall break down by severity: 1 Class I (may cause serious health issues), 0 Class II (may cause temporary health problems), and 0 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.
Raw Farm LLC recalls have affected AZ, CA, CO, FL, GA, IL, IN, MD, NV, TX. Check individual recall entries for specific distribution details.
Related
Recall data is sourced from the FDA openFDA enforcement database. Classifications reflect FDA severity ratings: Class I (dangerous), Class II (may cause temporary health problems), Class III (unlikely harmful).
The this entity record above pulls directly from the FDA openFDA enforcement-report API. What follows is the per-entity context — how this entity sits in the broader U.S. FDA food, drug, and device recalls distribution and which underlying factors drive the headline numbers.
Every number on this page links back to the FDA openFDA enforcement-report API; the methodology page describes the inputs, refresh cadence, and known limitations of the underlying data product.
For readers using this page as a decision input, the related-entity pages elsewhere on the site provide the comparison set. The most useful comparison for this entity is typically a peer within U.S. consumer-product recalls with similar size, similar exposure, or similar geography — not the national-level summary alone.