PlainRecalls
FDA Food Verify with FDA Food → Critical Class I Terminated

Xtra Butter Microwave Popcorn bags packaged in cardboard boxes labeled to be Jolly Time Healthy Pop 100's Kettle Corn 100 Calorie Singles, 3 1.2 oz (34 g) Net Wt 4.8 oz (136 g), American Pop Corn Co. Sioux City, Iowa

Reported: June 2, 2021 Initiated: May 12, 2021 #F-0624-2021 286 cases units

American Pop Corn Co issued this FDA Food recall on June 2, 2021. Classified as Critical severity (Class I). Approximately 286 cases units are affected. The recall was issued because: Buttered microwave popcorn bags were packaged inside a regular popcorn box which fails to declare the major food allerg…. This recall notice is sourced from official FDA Food enforcement records. Below you will find the complete product description, hazard information, remedy instructions, and related recalls from the same manufacturer or product category.

Recall Insight

This FDA Food action (record #F-0624-2021) was formally reported on June 2, 2021, with the manufacturer initiating the action on May 12, 2021. It is classified under Critical severity (Class I), with a current status of Terminated. American Pop Corn Co is listed as the recalling firm, operating out of Sioux City, IA. Federal records indicate 286 cases units are affected.

The documented reason for this recall is: Buttered microwave popcorn bags were packaged inside a regular popcorn box which fails to declare the major food allergen milk. Distribution data in the federal record shows the product reached: Distributed to distribution centers in CA, IA, KS, NE, and UT for final retail store distribution to potentially AZ, CA, CO, ID, IA, KS, MN, MO, MT, NE, NV, OR, SD, UT, WI and WY.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Food. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 5 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.

Recall Distribution by Severity Class

Severity1Class I (Critical)Class II (Moderate)Class III (Low)
Recall Distribution by Severity Class

Severity

Critical

Units Affected

286 cases

Related Recalls

6

6 from same agency

Product Description

Xtra Butter Microwave Popcorn bags packaged in cardboard boxes labeled to be Jolly Time Healthy Pop 100's Kettle Corn 100 Calorie Singles, 3 1.2 oz (34 g) Net Wt 4.8 oz (136 g), American Pop Corn Co. Sioux City, Iowa

Reason for Recall

Buttered microwave popcorn bags were packaged inside a regular popcorn box which fails to declare the major food allergen milk.

Details

Recalling Firm
American Pop Corn Co
Units Affected
286 cases
Distribution
Distributed to distribution centers in CA, IA, KS, NE, and UT for final retail store distribution to potentially AZ, CA, CO, ID, IA, KS, MN, MO, MT, NE, NV, OR, SD, UT, WI and WY.
Location
Sioux City, IA

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Critical (Class I)
Status Terminated
Recall number F-0624-2021
Date reported June 2, 2021
Date initiated May 12, 2021
Recalling firm American Pop Corn Co
Units affected 286 cases
Distribution Distributed to distribution centers in CA, IA, KS, NE, and UT for final retail store distribution to potentially AZ, CA, CO, ID, IA, KS, MN, MO, MT, NE, NV, OR, SD, UT, WI and WY.

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

286 cases units affected — limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units)
Large-scale (100K – 1M units)
Massive (≥1M units)

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

Frequently Asked Questions

What product was recalled?
Xtra Butter Microwave Popcorn bags packaged in cardboard boxes labeled to be Jolly Time Healthy Pop 100's Kettle Corn 100 Calorie Singles, 3 1.2 oz (34 g) Net Wt 4.8 oz (136 g), American Pop Corn Co. Sioux City, Iowa. Recalled by American Pop Corn Co. Units affected: 286 cases.
Why was this product recalled?
Buttered microwave popcorn bags were packaged inside a regular popcorn box which fails to declare the major food allergen milk.
Which agency issued this recall?
This recall was issued by the FDA Food on June 2, 2021. Severity: Critical. Recall number: F-0624-2021.
Where was the recalled product distributed?
Distribution: Distributed to distribution centers in CA, IA, KS, NE, and UT for final retail store distribution to potentially AZ, CA, CO, ID, IA, KS, MN, MO, MT, NE, NV, OR, SD, UT, WI and WY..
How do I check if my product is affected by a recall?
Check the product description and recall number (F-0624-2021) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Recall Context

Product recalls are issued when a manufacturer, distributor, or federal agency determines that a product poses a safety risk to consumers. This recall is classified as critical severity, meaning the product carries a reasonable probability of serious adverse health consequences or death. Across PlainRecalls, we track 83,000+ recalls from FDA, CPSC, and NHTSA to help consumers stay informed and act quickly when safety issues arise.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

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Data Sources

Data as of 2025. Source: FDA, CPSC, NHTSA, USDA FSIS federal recall databases.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
  • Source: USDA FSIS — Food Safety and Inspection Service (meat, poultry, and egg product recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

All federal data sources used on this page

Source: Federal recall agencies (FDA, CPSC, NHTSA, USDA FSIS) Aggregated multi-agency recall feeds · 2024 Recall data normalized across federal agency feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC, NHTSA, USDA FSIS).