Fresh Recalls

FDANot Yet Classified · Food · FDA event 99560; recall number pending · Recalled August 12, 2026

Blank Slate Creamery VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES recall — Blank Slate Creamery Production

Agency report date: August 12, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Blank Slate Creamery VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES
Company / brand
Blank Slate Creamery Production
Lot / serial / date codes
best by dates 11/23/26 and 1/9/27
Distribution
Ann Arbor and Brighton, MI at 3 store locations
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: undeclared egg

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Affected product: Blank Slate Creamery VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES

3. Open the official notice or contact

Official recall ID
Not yet assigned by the FDA — identified by FDA event ID 99560
Brand
Blank Slate Creamery Production
Classification
Not Yet Classified
Units affected
66 individual retail units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Ann Arbor, MI, United States
Firm address
7879 Jackson Rd, 48103-9559

Identifying details (verbatim from the notice)

Product codes / lots
best by dates 11/23/26 and 1/9/27
Distribution
Ann Arbor and Brighton, MI at 3 store locations
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
99560
Recall initiated
August 1, 2026
FDA report date
August 12, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved August 25, 2026 at 6:00 PM UTC.

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