U-BAKE Pie Crust
Reason Undeclared egg
U-BAKE Apple Pie recall
Recalled by Grand Central Bakery FRE Co Inc · Portland, OR, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Undeclared egg
Undeclared allergen: Egg
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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.
Quantity: 150 packages
Food: Fresh fruit Bread & bakery
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Expiration dates between 02/01/2025 and 04/17/2025
Where it was sold
Oregon Washington
FDA's distribution note: Distributed in OR and WA.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Grand Central Bakery FRE Co Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 25, 2024
- In FDA report of
- Nov 27, 2024
- Terminated
- Mar 17, 2026
- FDA recall number
- F-0217-2025 · event 95623
- Official record
- FDA enforcement report search
Also recalled with it (3 more products)
FDA files each product of one recall action separately; these share the same FDA event.
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