Zupan Enterprises, INC. Recall History
Zupan Enterprises, INC. has had 1 FDA-tracked food recall since 2016, 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 2016
- Class I (Most Serious)
- 1
- Most Common Reason
- Listeria contamination (1)
- Latest Recall
- Jun 15, 2016
- First Recorded Recall
- Jun 15, 2016
- States Affected
- IN, OR
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (1 Records)
Every Zupan Enterprises, 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 |
|---|---|---|---|
| Jun 15, 2016 | Macaroni Salad with Cheddar Cheese is packaged in a plast... | Class I | 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, Zupan Enterprises, INC. has 1 FDA food recall on record, including 1 Class I (dangerous) recall. There are no active recalls at this time.
Zupan Enterprises, INC. has no active recalls at this time. However, the brand has 1 historical recall. Always check this page for the latest recall status.
Zupan Enterprises, INC.'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.
Zupan Enterprises, INC. recalls have affected IN, OR. 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.
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.