Bonduelle USA INC. Recall History
Bonduelle USA INC. has had 2 FDA-tracked food recalls since 2021. 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
- 2
- Years in FDA Data
- Since 2021
- Class I (Most Serious)
- 0
- Most Common Reason
- Foreign material (2)
- Latest Recall
- Mar 16, 2021
- First Recorded Recall
- Mar 16, 2021
- States Affected
- FL
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (2 Records)
Every Bonduelle USA 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 |
|---|---|---|---|
| Mar 16, 2021 | El Sembrador Peas and Carrots, poly bags, 12/16 oz | Class II | Terminated |
| Mar 16, 2021 | EL Sembrador MIxed vegetables, Poly bags, 12/ 32 oz. | Class II | 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, Bonduelle USA INC. has 2 FDA food recalls on record, including 0 Class I (dangerous) recalls. There are no active recalls at this time.
Bonduelle USA INC. has no active recalls at this time. However, the brand has 2 historical recalls. Always check this page for the latest recall status.
Bonduelle USA INC.'s 2 recalls break down by severity: 0 Class I (may cause serious health issues), 2 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.
Bonduelle USA INC. recalls have affected FL. 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).
this entity is one of the data points covered by this site’s U.S. FDA food, drug, and device recalls dataset. The detail above comes directly from the FDA openFDA enforcement-report API; the context that follows situates the headline numbers against the broader distribution across U.S. consumer-product recalls.
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.