Gina Marie Bakery LLC Recall History
Gina Marie Bakery LLC has had 3 FDA-tracked food recalls since 2025. 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
- 3
- Years in FDA Data
- Since 2025
- Class I (Most Serious)
- 0
- Most Common Reason
- Undeclared allergens (3)
- Latest Recall
- Sep 10, 2025
- First Recorded Recall
- Sep 10, 2025
- States Affected
- CT
- Currently Active
- 3
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (3 Records)
Every Gina Marie Bakery LLC 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, 2025 | Vanilla Cookies with Raspberry Peach Jam | Class II | Active |
| Sep 10, 2025 | Toasted Cherry Biscotti | Class III | Active |
| Sep 10, 2025 | Italian Sesame Cookies | Class II | Active |
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, Gina Marie Bakery LLC has 3 FDA food recalls on record, including 0 Class I (dangerous) recalls. There are currently 3 active recalls.
Gina Marie Bakery LLC currently has 3 active recalls. Check the recall details above to see if your specific product is affected. If you have a recalled product, do not consume it.
Gina Marie Bakery LLC's 3 recalls break down by severity: 0 Class I (may cause serious health issues), 2 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.
Gina Marie Bakery LLC recalls have affected CT. 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.
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.