RecallHawk
Class III Recall

Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.

Prospector Popcorn, LLC

Summary

The FDA issued a Class III for Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz. by Prospector Popcorn, LLC. Reason: Inaccurately declared nutrients including Potassium (overstated), Calcium (overstated), and Iron (understated)..

Details

Source

Food Recall

External ID

H-1233-2026

Action Date

2026-08-26

Status

Ongoing

Category

food

Product Description

Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.

Lot/Code Info: UPC: 850073852224 All Best By date on or before July 10, 2027

Quantity Affected: 21,400 units (total)

Reason for Recall

Inaccurately declared nutrients including Potassium (overstated), Calcium (overstated), and Iron (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

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-1233-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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