Sspi Mid-Atlantic, INC Recall History
Sspi Mid-Atlantic, INC has had 1 FDA-tracked food recall 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
- 1
- Years in FDA Data
- Since 2021
- Class I (Most Serious)
- 0
- Most Common Reason
- Undeclared allergens (1)
- Latest Recall
- Sep 10, 2021
- First Recorded Recall
- Sep 10, 2021
- States Affected
- IN, VA
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (1 Records)
Every Sspi Mid-Atlantic, 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 |
|---|---|---|---|
| Sep 10, 2021 | 1. Dickies Seafood Cooked & Spiced Shrimp (12 oz) UPC 524... | 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, Sspi Mid-Atlantic, INC has 1 FDA food recall on record, including 0 Class I (dangerous) recalls. There are no active recalls at this time.
Sspi Mid-Atlantic, INC has no active recalls at this time. However, the brand has 1 historical recall. Always check this page for the latest recall status.
Sspi Mid-Atlantic, INC's 1 recall break down by severity: 0 Class I (may cause serious health issues), 1 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.
Sspi Mid-Atlantic, INC recalls have affected IN, VA. 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.
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.