Check the Batch
Class IITerminated in FDA datasetRecall initiated Sep 18, 2012

Popcorn Indiana Aged White Cheddar Popcorn 0.8 oz -

Recalling firm: Dale & Thomas Popcorn, LLC

Why it was recalled

Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono. This recall was expanded to the consumer level once L. mono was confirmed in…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 25, 2013.

Check your package

Compare the exact product and package details with the label you have.

ProductPopcorn Indiana Aged White Cheddar Popcorn 0.8 oz - UPC 843571004233 3.5 oz- UPC 843571000532 8 oz- UPC 843571000785 8.3 oz - UPC 843571002956 9 oz - UPC843571000785 Popcorn, Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA
Package size0.8 oz
UPC843571000785

FDA code information

3.5 oz 12228ENGA 2/11/2013 12233ENGA 2/16/2013 12242ENGA 2/25/2013 12244ENGA 2/27/2013 12254ENGA 3/9/2013 12255ENGA 3/10/2013 8 oz. 12222ENGA 2/5/2013 12228ENGA 2/11/2013 12235ENGA 2/18/2013 12243ENGA 2/26/2013 12244ENGA 2/27/2013 12254ENGA 3/9/2013 12255ENGA 3/10/2013 8.3 oz 12222ENGA 2/5/2013 12235ENGA 2/18/2013 12242ENGA 2/25/2013 12244ENGA 2/27/2013 Canada 9.3 oz. 12235ENGA 2/18/2013 12242ENGA 2/25/2013

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Popcorn Indiana Aged White Cheddar Popcorn 0.8 oz - UPC 843571004233 3.5 oz- UPC 843571000532 8 oz- UPC 843571000785 8.3 oz - UPC 843571002956 9 oz - UPC843571000785 Popcorn, Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA

Extracted codes and context

TypeCode / valueContext
UPC843571000785 UPC 843571000532 8 oz- UPC 843571000785 8.3 oz - UPC 843571002956 9 oz - UPC843571000785 Popcorn, Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA

Original FDA recall reason

Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono. This recall was expanded to the consumer level once L. mono was confirmed in finished product.

Recall details

Recall number
F-0580-2013
Event ID
63303
FDA status
Terminated
Initiated
Sep 18, 2012
Reported
Nov 7, 2012
Classified
Nov 1, 2012
Terminated
Sep 25, 2013
Quantity
398910 bags
Location
Englewood, NJ, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide, Canada

FDA source record · F-0580-2013

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.