Grand Central Bakery Fre CO INC Recall History
Grand Central Bakery Fre CO INC has had 2 FDA-tracked food recalls since 2024, 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 2024
- Class I (Most Serious)
- 2
- Most Common Reason
- Undeclared allergens (2)
- Latest Recall
- Oct 25, 2024
- First Recorded Recall
- Oct 25, 2024
- States Affected
- IN, OR, WA
- Currently Active
- 0
- Data Source
- FDA openFDA + USDA FSIS
Complete Recall List (2 Records)
Every Grand Central Bakery Fre CO 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 |
|---|---|---|---|
| Oct 25, 2024 | U-BAKE Chicken Pot Pie, frozen product and packaged in he... | Class I | Terminated |
| Oct 25, 2024 | U-BAKE Marionberry Pie, frozen product and packaged in LD... | 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, Grand Central Bakery Fre CO INC has 2 FDA food recalls on record, including 2 Class I (dangerous) recalls. There are no active recalls at this time.
Grand Central Bakery Fre CO INC has no active recalls at this time. However, the brand has 2 historical recalls. Always check this page for the latest recall status.
Grand Central Bakery Fre CO INC'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.
Grand Central Bakery Fre CO INC recalls have affected IN, OR, 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.
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.
Practical use of this page is in combination with the comparison and ranking pages elsewhere on the site, which surface the same data for this entity’s peers within U.S. consumer-product recalls. A single-entity reading without peer context can be misleading when an entity is an outlier on one axis but typical on another.