Tiffany Food Corp. Recall History
Tiffany Food Corp. has had 2 FDA-tracked food recalls since 2023, 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
- 2
- Years in FDA Data
- 2023–2024
- Class I (Most Serious)
- 1
- Most Common Reason
- Undeclared allergens (1)
- Latest Recall
- Apr 18, 2024
- First Recorded Recall
- Oct 19, 2023
- States Affected
- AZ, NJ, NY, TN, TX, PA
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (2 Records)
Every Tiffany Food Corp. 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 18, 2024 | Sweet Preserved Dried Plums; Farmer's Grange; Series Food... | Class III | Terminated |
| Oct 19, 2023 | Mini Fruit Jelly Cups; Assorted Flavor; UPC: 4 714379 320... | 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, Tiffany Food Corp. has 2 FDA food recalls on record, including 1 Class I (dangerous) recall. There are no active recalls at this time.
Tiffany Food Corp. has no active recalls at this time. However, the brand has 2 historical recalls. Always check this page for the latest recall status.
Tiffany Food Corp.'s 2 recalls break down by severity: 1 Class I (may cause serious health issues), 0 Class II (may cause temporary health problems), and 1 Class III (unlikely to cause harm). See the full recall history table above for specific reasons.
Tiffany Food Corp. recalls have affected AZ, NJ, NY, TN, TX, PA. 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.