RecallRadar
FDA · FoodClass I

Blank Slate Creamery Production food recall: Blank Slate Creamery VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE…

Undeclared allergens

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Terminated
Event ID
99560
Recall initiated
Aug 1, 2026
Classified by FDA
Aug 26, 2026
Posted in Enforcement Report
Aug 12, 2026
Terminated
Sep 9, 2026
Recalling firm
Blank Slate Creamery Production
Firm location
Ann Arbor, MI, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

undeclared egg

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Aug 1, 2026. FDA classified it 25 days later, on Aug 26, 2026. Distribution reported by FDA: Ann Arbor and Brighton, MI at 3 store locations

Recalled products (1)

  • H-1272-2026 Class I Terminated

    Blank Slate Creamery VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES, 4.5 oz clear plastic package

    Codes / lots: best by dates 11/23/26 and 1/9/27

    Quantity: 66 individual retail units

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 99560
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.