ModerateClass IITerminated

FDA Food recall · Reported November 7, 2012

Popcorn Indiana Drizzled Black & White Kettlecorn Net Wt. 6 oz. UPC 843571002345 Canada - Drizzled Black & White Kettlecorn Marbre Noir & Blanc Mais A Marmite Popcorn Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA

Q: Which agency issued this recall?

This recall was issued by the FDA Food on November 7, 2012. Severity: Moderate. Recall number: F-0586-2013.

Q: Where was the recalled product distributed?

Distribution: Nationwide, Canada.

Q: 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.

Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.

Recall #: F-0586-2013
Affected scope: 17664 units - US; 2,016 units - Canada
Initiated: September 18, 2012

Compiled from official public sources by the publisher. · Updated September 2026

Verify with FDA Food →

View my saved recalls

Dale & Thomas Popcorn, LLC recalled Popcorn Indiana Drizzled Black & White Kettlecorn Net Wt. 6 oz. UPC 843571002345 Canada… - a moderate-severity action.

Popcorn Indiana Drizzled Black & White Kettlecorn Net Wt. 6 oz. UPC 843571002345 Canada… was recalled by Dale & Thomas Popcorn, LLC in November 7, 2012. Reason: Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.. Check the official notice for the remedy. Verify recall #F-0586-2013 with the FDA Food before acting.

The recall

Dale & Thomas Popcorn, LLC issued this moderate-severity FDA Food recall-Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono..

Moderate
severity level: 18K units
affected scope: Class II
classification: November 7, 2012
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0586-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Product description

Popcorn Indiana Drizzled Black & White Kettlecorn Net Wt. 6 oz. UPC 843571002345 Canada - Drizzled Black & White Kettlecorn Marbre Noir & Blanc Mais A Marmite Popcorn Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA

Reason for recall

Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Moderate (Class II)
Status	Terminated
Recall number	F-0586-2013
Date reported	November 7, 2012
Date initiated	September 18, 2012
Recalling firm	Dale & Thomas Popcorn, LLC
Firm location	Englewood, NJ
Affected scope	17664 units - US; 2,016 units - Canada
Distribution	Nationwide, Canada

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

Scale of Impact

17664 units - US; 2,016 units - Canada units affected - limited or regional distribution scale.

Regional (<10K units) -

Multi-state (10K – 100K units) ✓ This recall

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.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

Check the recall number (F-0586-2013) and product description against the item you own. Search the archive
Confirm the current status with FDA Food before acting, recall details can be updated.
Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled? ▼

Why was this product recalled? ▼

Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.

Which agency issued this recall? ▼

This recall was issued by the FDA Food on November 7, 2012. Severity: Moderate. Recall number: F-0586-2013.

Where was the recalled product distributed? ▼

Distribution: Nationwide, Canada.

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.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Similar severity · nearest report date

Same archive severity grade (Moderate), closest by report date among other firms and states.

High Pressure Scuba Diving Hoses Recalled… 2012-11-07 Sauder Woodworking Company Recalls Gruga … 2012-11-07 UP & UP brand, kid's foaming hand sanitiz… 2012-11-07 UP & UP brand, kid's foaming hand sanitiz… 2012-11-07

Similar Food · nearest report date

Same product category, closest by report date among other firms and states (deduped against the severity set).

Mega Raw Oriental Produce Wholesaler- Val… 2012-11-07 Mega Raw Oriental Produce Wholesaler- Vir… 2012-11-07 Natural Value Raw Peanuts, 30 lb Item num… 2012-11-07 Sunland Roasted Valencia Peanuts, 2 oz, U… 2012-11-07

Compare this recall with Grade A White In-shell Chicken eggs packaged in the followi… → · All Food recalls

This recall: FDA Food, reported November 7, 2012. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026