Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz
Summary
The FDA issued a Class III for Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz by Prospector Popcorn, LLC. Reason: Inaccurately declared nutrients including Potassium (overstated) and Calcium (overstated)..
Details
Source
Food Recall
External ID
H-1234-2026
Action Date
2026-08-26
Status
Ongoing
Category
food
Product Description
Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz
Lot/Code Info: 1.5 oz size UPC: 850073852354; all best by dates on or before July 10, 2027 3.5 oz. size UPC: 850073852293; all best by dates on or before July 10, 2027
Quantity Affected: 21,400 units (total)
Reason for Recall
Inaccurately declared nutrients including Potassium (overstated) and Calcium (overstated).
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 III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
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 III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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-1234-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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