Class ITerminatedVoluntary: Firm initiated
Blank Slate Creamery Production: food recall H-1272-2026
Blank Slate Creamery Production of Ann Arbor, MI recalled Blank Slate Creamery VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES, 4.5 oz clear plastic package. Reason: undeclared egg. The FDA listed it as Class I in its Enforcement Report dated Aug 12, 2026; distribution: Michigan.
Record status as published: Terminated (terminated Sep 9, 2026). 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
- Blank Slate Creamery VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES, 4.5 oz clear plastic package
- Product quantity
- 66 individual retail units
- Reason for recall
- undeclared egg
- Codes, lots and dates on the package
- best by dates 11/23/26 and 1/9/27
- Distribution pattern
- Ann Arbor and Brighton, MI at 3 store locations
- Recalling firm
- Blank Slate Creamery Production, Ann Arbor, MI
- 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
Advertisement
Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Aug 1, 2026 |
| Classified by the FDA | Aug 26, 2026 |
| Published in the Enforcement Report | Aug 12, 2026 |
| Terminated | Sep 9, 2026 |
Advertisement
OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-1272-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.