Carrot Bundt Cake - Net Weight 4 lbs Contains: Wheat, Soy, Milk, Eggs, Tree Nuts No UPC
Summary
The FDA issued a Class I for Carrot Bundt Cake - Net Weight 4 lbs Contains: Wheat, Soy, Milk, Eggs, Tree Nuts by Doan's Dessert And Coffee. Reason: Undeclared allergen ingredient (Wheat) in Ready-to-eat frozen cakes..
Details
Source
Food Recall
External ID
H-0137-2026
Action Date
2025-11-05
Status
Terminated
Category
food
Product Description
Carrot Bundt Cake - Net Weight 4 lbs Contains: Wheat, Soy, Milk, Eggs, Tree Nuts No UPC
Lot/Code Info: Lot Code: N/A
Quantity Affected: 4,050 across both recalled products
Reason for Recall
Undeclared allergen ingredient (Wheat) in Ready-to-eat frozen cakes.
Distribution
Two retail locations with nationwide distribution: New York and California. Product is also distributed from the stores walk-up counter.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-01
Company
Woodland Hills, CA
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 62 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Doan's Dessert And Coffee has 2 FDA actions in our database, including 2 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 (Doan's Dessert And Coffee) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Doan's Dessert And Coffee have FDA actions?
Doan's Dessert And Coffee has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0137-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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