The Earl of Sandwiches Recall History
The Earl of Sandwiches has had 2 FDA-tracked food recalls since 2021, including 2 Class I recalls (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
- Since 2021
- Class I (Most Serious)
- 2
- Most Common Reason
- Undeclared allergens (2)
- Latest Recall
- Sep 16, 2021
- First Recorded Recall
- Sep 16, 2021
- States Affected
- MN, UT, WA
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (2 Records)
Every The Earl of Sandwiches 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 |
|---|---|---|---|
| Sep 16, 2021 | Earle of Sandwiches Mild Smoked Jalapeno Sub, Smoked Jala... | Class I | Terminated |
| Sep 16, 2021 | Duke of Earle Spicy Chicken Sub, Seasoned Chicken with Pe... | 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, The Earl of Sandwiches has 2 FDA food recalls on record, including 2 Class I (dangerous) recalls. There are no active recalls at this time.
The Earl of Sandwiches has no active recalls at this time. However, the brand has 2 historical recalls. Always check this page for the latest recall status.
The Earl of Sandwiches's 2 recalls break down by severity: 2 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.
The Earl of Sandwiches recalls have affected MN, UT, WA. 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.