RecallHawk
Class II Recall

Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO popcorn, brown sugar, corn syru

Prospector Popcorn, LLC

Summary

The FDA issued a Class II for Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: by Prospector Popcorn, LLC. Reason: Products contain undeclared soy, specifically soy lecithin..

Details

Source

Food Recall

External ID

H-0779-2026

Action Date

2026-05-20

Status

Ongoing

Category

food

Product Description

Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO popcorn, brown sugar, corn syrup, butter, vanilla, baking soda, sea salt, white chocolate (sugar, palm kernel fat, skimmed milk powder [12%], emulsifier [lecithins], natural vanilla flavoring), dark chocolate (sugar, palm kernel fat, fat reduced cocoa powder [20%], emulsifiers [lecithins], natural vanilla flavoring), pretzels (flour, water, salt, malt, dextrose, canola oil, yeast, soda), tofee bits (sugar, butter, almonds), coarse sea salt.; CONTAINS: MILK, TREE NUTS (ALMONDS), WHEAT; Produced in a facility that is shared with gluten, nuts, dairy, and soy.; Manufactured by: Prospector Popcord, LLC, Ridgefield, CT 06877; UPC: 850073852125

Lot/Code Info: Expiration dates August 5 - October 24, 2026

Quantity Affected: 140 - 3.5 oz bags

Reason for Recall

Products contain undeclared soy, specifically soy lecithin.

Distribution

CT and NY

Type: Voluntary: Firm initiated

Recall Initiated: 2026-04-28

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 97 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Prospector Popcorn, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Prospector Popcorn, LLC have FDA actions?

This is the only FDA action we have on record for Prospector Popcorn, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0779-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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