FDA Upgrades Michigan Dairy-Free Ice Cream Sandwich Recall Over Undeclared Eggs

The FDA has classified a Michigan dairy-free ice cream sandwich recall as Class I after the product was linked to aquafaba powder that may contain undeclared egg.

A popular dairy-free frozen dessert sold in parts of Michigan is now the subject of a higher-level food safety alert after the U.S. Food and Drug Administration (FDA) classified the recall as a Class I recall.

The recall involves Blank Slate Creamery's Frozen Dessert Coconut Fudge sandwiches, a non-dairy frozen treat sold at several retail locations in Ann Arbor and Brighton, Michigan. The concern is the possible presence of undeclared egg, an ingredient that can pose a serious risk to people with an egg allergy.

The product was voluntarily withdrawn after a supplier ingredient was found to potentially contain egg even though it was marketed as an egg substitute.

Why Was the Dairy-Free Ice Cream Sandwich Recalled?

According to the FDA, Blank Slate Creamery's recall is connected to Rooted in Rare Aquafaba Powder, an ingredient supplied to the dessert maker.

Aquafaba is commonly used as an egg substitute and is made from cooked chickpeas or other legumes. Because it can help provide structure and texture in foods, it is sometimes used in place of egg whites in vegan and dairy-free recipes.

However, the FDA reported that certain Rooted in Rare Aquafaba Powder products may contain undeclared egg.

The underlying aquafaba recall was announced by 529 Commerce LLC on July 29, 2026, and published by the FDA on July 30. The company recalled 3,860 units of its 4-ounce and 12-ounce Rooted in Rare Aquafaba Powder products because they could contain undeclared egg.

The FDA said the recall was initiated after a consumer reported an allergic reaction. At the time of the FDA announcement, no other illness reports had been received.

What Dairy-Free Ice Cream Sandwiches Are Affected?

The Blank Slate Creamery recall applies to its Frozen Dessert Coconut Fudge sandwiches.

The recalled desserts were packaged individually in clear plastic containers and were sold through retail locations in the Ann Arbor and Brighton areas of Michigan.

Consumers who may have purchased the product should carefully check their packages and avoid eating the dessert if they believe it is part of the recalled production.

The recall is especially important for consumers who have an egg allergy or a severe sensitivity to egg.

People with egg allergies can experience reactions after consuming even relatively small amounts of an allergen. Reactions can range from mild symptoms to potentially life-threatening anaphylaxis.

FDA Class I Recall Explained

The FDA's decision to classify the incident as Class I makes the recall particularly significant.

A Class I recall represents the FDA's highest risk classification. It is used when there is a reasonable probability that exposure to a violative product could result in serious adverse health consequences or death.

That classification does not mean that every person who eats the recalled dessert will become sick. Instead, it reflects the potential severity of the hazard, particularly for people who are allergic to the undeclared ingredient.

The FDA uses other classifications for recalls involving lower levels of risk. Class II recalls generally involve products that could cause temporary or medically reversible health effects, while Class III recalls generally concern violations that are unlikely to cause adverse health consequences.

What Is the Connection to Rooted in Rare Aquafaba Powder?

The issue began with the ingredient used in the frozen dessert.

The FDA said the recalled Rooted in Rare Aquafaba Powder was sold in 4-ounce and 12-ounce flexible foil pouches. The products carried UPC numbers 199284530959 for the 4-ounce package and 199284306226 for the 12-ounce package.

The FDA's recall notice states that the affected aquafaba products had best-by dates of December 14, 2026, and December 12, 2027. The powder was distributed nationwide through Amazon and directly to consumers through the company's website between June 2025 and July 2026.

The company said it had ended its relationship with the supplier associated with the issue.

Because the recalled ingredient had been used in a finished frozen dessert, the supplier-level recall resulted in a downstream recall involving the Coconut Fudge sandwiches.

What Should Consumers Do?

Consumers who purchased the affected dairy-free frozen dessert should not eat it if they have an egg allergy or sensitivity.

Anyone who believes they purchased a recalled item should follow the recall instructions provided by the retailer or manufacturer. Consumers can also contact Blank Slate Creamery for information about the recalled dessert.

The FDA advises consumers to take food allergen recalls seriously, particularly when a major allergen is not identified on the product label.

If someone with an egg allergy develops symptoms after eating a recalled product, they should seek appropriate medical attention. Anyone experiencing signs of a severe allergic reaction, such as difficulty breathing, swelling of the throat or tongue, or other symptoms of anaphylaxis, should seek emergency medical care immediately.

Why Undeclared Egg Is a Serious Food Safety Issue

Egg is one of the major food allergens that U.S. food manufacturers must identify when it is present as an ingredient.

The FDA recognizes nine major food allergens: milk, eggs, fish, crustacean shellfish, tree nuts, peanuts, wheat, soybeans and sesame.

For most consumers, an undeclared egg ingredient may not create a health concern. For someone with an egg allergy, however, accidental exposure can result in an allergic reaction.

This is particularly relevant to products promoted as dairy-free or using plant-based ingredients. Consumers may reasonably expect such products to avoid certain animal-derived ingredients, but dairy-free does not automatically mean egg-free.

That distinction is important when shopping for foods intended for people with food allergies.

What the FDA Recall Means for Consumers

The elevated recall classification highlights the importance of checking food recall announcements even when a product appears to be a specialty or alternative food.

Consumers who regularly purchase dairy-free, vegan or allergen-conscious products should continue reading labels and monitoring recall notices. Ingredient formulations and supplier relationships can change, and a product's marketing description does not necessarily establish that it is free from every allergen.

In this case, the concern arose from an ingredient that was intended to function as an egg substitute.

The FDA's public recall notice confirms that the aquafaba powder itself was recalled because it may contain undeclared egg, and the agency specifically warned that people with an egg allergy or severe sensitivity could face serious or life-threatening reactions.

Key Facts About the Recall

Product: Blank Slate Creamery Frozen Dessert Coconut Fudge

Product category: Dairy-free or non-dairy frozen dessert

Issue: Potential undeclared egg

Location: Michigan

Affected areas: Ann Arbor and Brighton

Recall classification: Class I

Related ingredient: Rooted in Rare Aquafaba Powder

Aquafaba recall: 3,860 units

Aquafaba sizes: 4 ounces and 12 ounces

FDA aquafaba recall date: July 30, 2026

Consumers should rely on official recall information and product identification details rather than assuming that all products from the manufacturer are affected.

Bottom Line

The Michigan dairy-free ice cream sandwich recall has been elevated to a Class I recall because the affected Coconut Fudge dessert may contain undeclared egg. The issue is linked to recalled Rooted in Rare Aquafaba Powder, an ingredient that was intended to serve as an egg substitute.

While the risk is primarily significant for people with an egg allergy or severe sensitivity, consumers should check recall information carefully before eating a potentially affected product.

For the latest product identification details and official safety information, consumers should consult the FDA's recall notices and follow instructions from the manufacturer or retailer.

Sources

• U.S. Food and Drug Administration, "529 Commerce LLC Recalls Rooted in Rare Brand Aquafaba Powder Due to Undeclared Eggs."
• U.S. Food and Drug Administration, Enforcement Report, Event 99560.

Disclaimer

This article is provided for general informational purposes and is not medical advice. Recall information can change as manufacturers and government agencies provide updates. Consumers should verify product details and recall status through official FDA announcements and the manufacturer before consuming a potentially affected food. People with known food allergies should follow advice from their healthcare professionals and seek emergency medical attention for symptoms of a severe allergic reaction.