Summary
The FDA issued a Class II for Prospector Popcorn Chocolate Mocha Gourmet Popcorn 1.5 oz. by Prospector Popcorn, LLC. Reason: Inaccurately declared nutrients including Carbohydrates (understated) and Cholesterol (understated)..
Details
Source
Food Recall
External ID
H-1232-2026
Action Date
2026-08-26
Status
Ongoing
Category
food
Product Description
Prospector Popcorn Chocolate Mocha Gourmet Popcorn 1.5 oz.
Lot/Code Info: All Best By date on or before July 10, 2027. UPC Codes: 850073852392
Quantity Affected: 21,400 units (total)
Reason for Recall
Inaccurately declared nutrients including Carbohydrates (understated) and Cholesterol (understated).
Distribution
AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-07-15
Company
Ridgefield, CT
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 53 food recalls issued in the same week, part of 82 food-related FDA actions this month.
Prospector Popcorn, LLC has 5 FDA actions in our database, including 5 recalls.
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?
Prospector Popcorn, LLC has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1232-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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