Blank Slate Creamery recalls vegan coconut fudge sandwiches due to undeclared egg in some products. Consumers should check best by dates and stop using if concerned.
“Blank Slate Creamery Vegan Coconut Fudge Sandwiches Recall: Undeclared Egg Hazard.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/686174-blank-slate-creamery-vegan-coconut-fudge-sandwiches-recall-undeclared-egg. Based on FDA recall #H-1272-2026.
The FDA announced on Aug. 1, 2026, that Blank Slate Creamery Production voluntarily recalled its Vegan Non-Dairy Frozen Dessert Coconut Fudge Sandwiches due to an undeclared egg hazard. Consumers should check their products for the specified best-by dates and contact the company for a refund.
Distribution: Sold at 3 store locations in Ann Arbor and Brighton, MI
The hazard
The product contains undeclared egg, which poses a risk to individuals with egg allergies. According to the FDA, this is a Class I recall, indicating a reasonable probability that the food will cause serious adverse health consequences or death.
Context
GovInfoNow's records show other recent recalls involving undeclared egg allergens include the Kerry KC Everyday Mac & Cheese Recall on July 29, 2026, and the House of Flavors Vanilla Ice Cream Recall on Feb. 26, 2026. Additionally, Jaime's Foods issued a Jalapeno Ranch recall for undeclared egg allergen risk on Aug. 5, 2026.
How to tell if you have this one
Check for the 4.5 oz clear plastic package with best by dates 11/23/26 or 1/9/27. The product is labeled as vegan non-dairy frozen dessert.
Brand
Blank Slate Creamery
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Dates
Look for best by dates 11/23/26 or 1/9/27 on the 4.5 oz clear plastic package.
Stop Using If Concerned
If you have eaten the product, contact a healthcare provider or follow your doctor's advice for possible allergic reactions.
Where it went and when
Where it was distributed
Distributed in Michigan.
Listed by the agency
Not listed
FDA distribution: “Ann Arbor and Brighton, MI at 3 store locations” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Michigan.
Recall timeline
FDA terminated this recall 39 days after the firm started it.
1Firm started the recall
2Published in FDA’s Enforcement Report
3FDA classified it Class I
4Added to GovInfoNow
5FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #H-1272-2026 (August 1, 2026)
Plain-language summary written by qwen3:4b on September 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.