Rizo Lopez Foods, INC. DBA Don Francisco Cheese Recall History
Rizo Lopez Foods, INC. DBA Don Francisco Cheese has had 1 FDA-tracked food recall since 2024, 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 2024
- Class I (Most Serious)
- 1
- Most Common Reason
- Listeria contamination (1)
- Latest Recall
- Jan 11, 2024
- First Recorded Recall
- Jan 11, 2024
- States Affected
- 20 states (nationwide)
- Currently Active
- 1
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (1 Records)
Every Rizo Lopez Foods, INC. DBA Don Francisco Cheese 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 |
|---|---|---|---|
| Jan 11, 2024 | 365 Whole Foods Market Ricotta Part Skim 15 oz. UPC 9-948... | 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, Rizo Lopez Foods, INC. DBA Don Francisco Cheese has 1 FDA food recall on record, including 1 Class I (dangerous) recall. There is currently 1 active recall.
Rizo Lopez Foods, INC. DBA Don Francisco Cheese 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.
Rizo Lopez Foods, INC. DBA Don Francisco Cheese'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.
Rizo Lopez Foods, INC. DBA Don Francisco Cheese recalls have affected 20 states (nationwide distribution). 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).
For this entity, the underlying data on this page comes from the FDA openFDA enforcement-report API. The breakdown above is the federal record; the paragraphs below add the per-entity context that makes the headline numbers usable for a real decision rather than just a data lookup.
The methodology behind every numeric value on this page is publicly documented on the the FDA openFDA enforcement-report API portal and described in detail on this site’s methodology page. Refresh cadence varies by underlying series; the page surfaces the as-of date for each number so readers can trace any figure back to the source release.
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.