Prospector Popcorn, LLC recalls Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz
Prospector Popcorn, LLC started this recall on July 15, 2026. The FDA classified it as Class III, the least serious category: eating the product is not likely to cause health problems, but it breaks labeling or manufacturing rules. It was distributed in 45 states. We consider this recall active, so check your kitchen if you buy this brand.
- Status
- Active
- Recall started
- July 15, 2026
- Company
- Prospector Popcorn, LLC
- Classification
- Class III (unlikely to cause health problems)
- Where sold
- Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, District of Columbia, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin
- Quantity
- 21,400 units (total); 21,400 units (total); 21,400 units (total); 21,400 units (total)
Reason for recall (official wording)
Inaccurately declared nutrients including Potassium (overstated) and Calcium (overstated).
Recalled products (official wording)
- Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz
- Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.
- Prospector Popcorn Chocolate Mocha Gourmet Popcorn 1.5 oz.
- Prospector Popcorn Belgian Chocolate Toffee Gourmet Popcorn 3.5oz
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.
What to do
Compare the brand, size, lot code and dates on your package with the details above. If they match, do not eat it. Throw it away or return it to the store. Contact a healthcare provider if you feel unwell. Step-by-step guide.
Source: FDA Enforcement Report (openFDA), event 99434.