San Gennaro Foods, INC Recall History
San Gennaro Foods, INC has had 3 FDA-tracked food recalls since 2017. 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
- 3
- Years in FDA Data
- Since 2017
- Class I (Most Serious)
- 0
- Most Common Reason
- N/A
- Latest Recall
- Oct 13, 2017
- First Recorded Recall
- Oct 13, 2017
- States Affected
- 18 states (nationwide)
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (3 Records)
Every San Gennaro Foods, INC 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 |
|---|---|---|---|
| Oct 13, 2017 | Traditional Polenta, San Gennaro brand, Pre-cooked Ready ... | Class III | Terminated |
| Oct 13, 2017 | Sun-Dried Tomato Polenta, Melissa's brand, Shelf stable, ... | Class III | Terminated |
| Oct 13, 2017 | Red & Black Quinoa Organic Polenta, Ancient Harvest brand... | Class III | Terminated |
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, San Gennaro Foods, INC has 3 FDA food recalls on record, including 0 Class I (dangerous) recalls. There are no active recalls at this time.
San Gennaro Foods, INC has no active recalls at this time. However, the brand has 3 historical recalls. Always check this page for the latest recall status.
San Gennaro Foods, INC's 3 recalls break down by severity: 0 Class I (may cause serious health issues), 0 Class II (may cause temporary health problems), and 3 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.
San Gennaro Foods, INC recalls have affected 18 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).
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.
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.