FDA Issues Class II Recall for Gourmet Popcorn Due to Undeclared Soy Allergen

May 18, 2026 USA

Popcorn Recalled Over Multiple Undeclared Allergens | Food Manufacturing

The U.S. Food and Drug Administration (FDA) has classified a recall of gourmet popcorn products from Prospector Popcorn as a Class II recall due to the presence of an undeclared soy allergen.

The recall affects a limited batch of Belgian Chocolate Toffee-flavored popcorn after it was discovered that the product contained soy lecithin that was not declared on the label. The recall was initially announced voluntarily by the company on April 28, 2026, and received its Class II risk classification from the FDA on May 14, 2026.

Recalled Product Details

Consumers are advised to check for the following recalled product:

  • Belgian Chocolate Toffee-Flavored Popcorn
    Package Quantity: 140 bags
    Expiration Dates: Between August 5, 2026 and October 24, 2026
    UPC Code: 850073852125

The recalled popcorn products were distributed in Connecticut and New York.

Why the Product Was Recalled

According to the company, a substitute chocolate ingredient supplied by a vendor contained soy lecithin, which required allergen labeling under FDA regulations. Soy is recognized as one of the nine major food allergens in the United States.

Although soy lecithin is considered safe for general consumption, individuals with soy allergies may experience allergic reactions if exposed to undeclared soy ingredients.

Health Risks Associated With Soy Allergies

Food allergies can trigger symptoms ranging from mild to severe. Common symptoms may include:

  • Hives or skin rash
  • Swelling of lips, face, or throat
  • Stomach pain, nausea, vomiting, or diarrhea
  • Wheezing or breathing difficulties
  • Dizziness or fainting

In severe cases, exposure can lead to anaphylaxis, a potentially life-threatening allergic reaction requiring immediate medical attention.

As of May 14, 2026, no illnesses or allergic reactions related to the recalled popcorn had been reported.

Company Statement

Ryan Wenke stated that the company acted quickly after discovering the issue and worked directly with the FDA to initiate the recall. The substitute ingredient linked to the undeclared allergen has since been removed from production.

The company also reiterated its commitment to food safety and its mission of supporting employment opportunities for people with disabilities.

What Consumers Should Do

Consumers who purchased the recalled popcorn are advised not to consume the product. Affected items should be discarded or returned to the place of purchase.

Individuals who experience allergic symptoms after consuming the product should seek immediate medical attention.

Source: US FDA

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