Class IOngoingVoluntary: Firm initiated
The Better Bakehouse Snack Company: food recall H-0011-2027
The Better Bakehouse Snack Company of Las Vegas, NV recalled Donutful Chocolate Dipped Vanilla Cake Donuts - 7.05oz/10ct.Case Configuration 5 count carton, 6 cartons per case. UPC… Reason: Undeclared Milk. The FDA listed it as Class I in its Enforcement Report dated Oct 14, 2026; distribution: nationwide.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Donutful Chocolate Dipped Vanilla Cake Donuts - 7.05oz/10ct.Case Configuration 5 count carton, 6 cartons per case. UPC 850041392103. Paperboard carton containing 5 individually wrapped packages of two donuts each. UPC: 850041392103. The Better Bakehouse Snack Co. 3651 Lindell Rd, Suite D700 Las Vegas, NV 89103
- Product quantity
- 10,602 consumer units
- Reason for recall
- Undeclared Milk.
- Codes, lots and dates on the package
- Lot # 26078 BEST BY: 09/15/2026
- Distribution pattern
- Product was distributed nationwide.
- Recalling firm
- The Better Bakehouse Snack Company, Las Vegas, NV
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Aug 17, 2026 |
| Classified by the FDA | Oct 6, 2026 |
| Published in the Enforcement Report | Oct 14, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0011-2027 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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