Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO…
Prospector Popcorn, LLC recalled this product and the FDA reported the enforcement action on 20 May 2026 as Class II. The recall was initiated by the firm. Products contain undeclared soy, specifically soy lecithin.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- 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
- UPC
- 850073852125
- Reason for recall
- Products contain undeclared soy, specifically soy lecithin.
- Recalling firm
- Prospector Popcorn, LLC
- Firm location
- Ridgefield, Connecticut, United States
- Classification
- Class II
- Status
- Completed
- Recall number
- H-0779-2026
- Quantity
- 140 - 3.5 oz bags
- Distribution
- CT and NY
- Initiated
- 28 April 2026
- Reported by FDA
- 20 May 2026
- Firm notified by
- Product codes
- Expiration dates August 5 - October 24, 2026
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
- The distribution pattern names 2 states, and the FDA published the enforcement report 3 weeks after the firm began the recall.
- Dairy recalls split between pathogen contamination in products that skipped or under-ran pasteurisation and undeclared milk in products that should never have contained it, which is the same allergen viewed from two directions.
Named in the distribution pattern: Connecticut, New York. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.
What this recall was for
Undeclared allergens
An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.
A preventive controls plan covers an undeclared allergen under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(2)
- Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
- 21 CFR 101.4
- Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
The allergens named in this record: soy.
Filed under milk and dairy, nuts and seeds, snacks and confectionery, sauces, dips and condiments, spices and seasonings, grains, flour and pasta and beverages and juice. A product can sit in more than one.
Other milk and dairy recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Prospector Popcorn, LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2026-08-26 | Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz | Prospector Popcorn, LLC | Inaccurately declared nutrients including Potassium (overstated) and Calcium (overstated). | Class III |
| 2026-08-26 | Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz. | Prospector Popcorn, LLC | Inaccurately declared nutrients including Potassium (overstated), Calcium (overstated), and Iron (understated). | Class III |
| 2026-08-26 | Prospector Popcorn Chocolate Mocha Gourmet Popcorn 1.5 oz. | Prospector Popcorn, LLC | Inaccurately declared nutrients including Carbohydrates (understated) and Cholesterol (understated). | Class II |
| 2026-08-26 | Prospector Popcorn Belgian Chocolate Toffee Gourmet Popcorn 3.5oz | Prospector Popcorn, LLC | Inaccurately declared nutrients including Iron (understated), and Vitamin D (overstated). | Class III |
All 5 records for Prospector Popcorn, LLC
All 2026 recalls · All FDA food recall data
21 CFR 117.135(c)(2) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.