Class IITerminated in FDA datasetRecall initiated Sep 18, 2012

Popcorn Indiana Caramel Popcorn Net Wt. 7.4 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.

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 Caramel Popcorn Net Wt. 7.4 oz. UPC 843571003045 Net Wt. 8 oz - UPC 843571002369 Popcorn Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA
Package size7.4 oz
UPC843571002369, 843571003045

FDA code information

7.4 oz. 12233ENGA 2/16/2013 12257ENGA 3/12/2013 8.0 oz. 12221ENGA 2/4/2013 12233ENGA 2/16/2013 12248ENGA 3/3/2013

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Full FDA record and distribution details

Original product description

Popcorn Indiana Caramel Popcorn Net Wt. 7.4 oz. UPC 843571003045 Net Wt. 8 oz - UPC 843571002369 Popcorn Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA

Extracted codes and context

TypeCode / valueContext
UPC843571002369n Indiana Caramel Popcorn Net Wt. 7.4 oz. UPC 843571003045 Net Wt. 8 oz - UPC 843571002369 Popcorn Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA
UPC843571003045Popcorn Indiana Caramel Popcorn Net Wt. 7.4 oz. UPC 843571003045 Net Wt. 8 oz - UPC 843571002369 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.

Recall details

Recall number
F-0587-2013
Event ID
63303
FDA status
Terminated
Initiated
Sep 18, 2012
Reported
Nov 7, 2012
Classified
Nov 1, 2012
Terminated
Sep 25, 2013
Quantity
18054 units
Location
Englewood, NJ, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide, Canada

FDA source record · F-0587-2013

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

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