Class IFood recall: undeclared egg
U-BAKE Apple Pie, frozen product and 3 more products
Grand Central Bakery FRE Co Inc, of Portland, OR, began recalling these 4 products on . FDA classified the recall as Class I on .
Why it was recalled
In FDA’s words:
Undeclared egg
The allergen tags on this page are ours, matched from FDA’s words above.
The 4 products
U-BAKE Apple Pie, frozen product
U-BAKE Apple Pie, frozen product and packaged in LDPE bag, net wt. 2lbs. 9oz. Made by Grand Central Baking Company. Label declares Wheat and Milk.
- Codes and dates
- Expiration dates between 02/01/2025 and 04/17/2025
- Quantity
- 150 packages
- Class
- Class I
- Recall number
- F-0217-2025
U-BAKE Pie Crust (Pastry Round), frozen product
U-BAKE Pie Crust (Pastry Round), frozen product and packaged in LDPE bag, 2-10.5 inch pie crust per package, net wt. 20oz. Made by Grand Central Baking Company. Label declares Wheat and Milk. Bulk pie dough rolls, packaged in plastic wrap and parchment paper, net wt. 10lbs. Made by Grand Central Baking Company. There is no label added for the bulk pie dough. 10lb. package does not sold directly to consumer.
- Codes and dates
- Pie Crust 20oz: Expiration dates between 02/01/2025 and 04/17/2025. Bulk Pie Dough: Product is labeled with manufacturing dates between 8/1/24 and 10/17/24
- Quantity
- 1450/20oz. packages and 310 packages of bulk pie dough
- Class
- Class I
- Recall number
- F-0218-2025
U-BAKE Marionberry Pie, frozen product
U-BAKE Marionberry Pie, frozen product and packaged in LDPE bag, net wt. 2lbs. 4oz. Made by Grand Central Baking Company. Label declares Wheat and Milk.
- Codes and dates
- Expiration dates between 02/01/2025 and 04/17/2025
- Quantity
- 336 packages
- Class
- Class I
- Recall number
- F-0219-2025
U-BAKE Chicken Pot Pie, frozen product
U-BAKE Chicken Pot Pie, frozen product and packaged in heat-sealable polypropylene film. Net wt. 11.5oz. Made by Grand Central Baking Company. Label declares Wheat and Milk.
- Codes and dates
- Expiration dates between 11/1/2024 and 1/17/2025.
- Quantity
- 2637 packages
- Class
- Class I
- Recall number
- F-0220-2025
Where it was distributed
In FDA’s words:
Distributed in OR and WA.
What Class I means
In FDA’s definitions, a Class I recall is one where: there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. FDA’s recall definitions
If you have this product
- FDA’s enforcement report doesn’t say what to do with a recalled product. FDA posts some companies’ recall announcements on its Recalls, Market Withdrawals and Safety Alerts page; not every recall has one.
- FDA doesn’t update a recall’s status after classifying it, so this page can’t tell you whether the recall is still open.
- If someone has a serious allergic reaction, call 911. Signs of a serious reaction
Source
FDA’s Enforcement Report, read through openFDA. This recall first appeared in the report of . openFDA asks that its data not be relied on for decisions about medical care. AllergyNest isn’t affiliated with or endorsed by FDA.