RecallHawk
Class I Recall

U-BAKE Chicken Pot Pie, frozen product and packaged in heat-sealable polypropylene film. Net wt. 11.5oz. Made by Grand

Grand Central Bakery FRE Co Inc

Summary

The FDA issued a Class I for U-BAKE Chicken Pot Pie, frozen product and packaged in heat-sealable polypropyle by Grand Central Bakery FRE Co Inc. Reason: Undeclared egg.

Details

Source

Food Recall

External ID

F-0220-2025

Action Date

2024-11-27

Status

Terminated

Category

food

Product Description

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.

Lot/Code Info: Expiration dates between 11/1/2024 and 1/17/2025.

Quantity Affected: 2637 packages

Reason for Recall

Undeclared egg

Distribution

Distributed in OR and WA.

Type: Voluntary: Firm initiated

Recall Initiated: 2024-10-25

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 25 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Grand Central Bakery FRE Co Inc has 4 FDA actions in our database, including 4 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Grand Central Bakery FRE Co Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Grand Central Bakery FRE Co Inc have FDA actions?

Grand Central Bakery FRE Co Inc has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0220-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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