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Class IITerminated in FDA datasetRecall initiated Sep 18, 2012

Popcorn Indiana Kettlecorn Net Wt. 9.75 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 Kettlecorn Net Wt. 9.75 oz UPC 84357100050 Net Wt. 14 oz. UPC 843571000693 Net Wt. 8 pack bag 0.7 oz. UPC 843571001676 Popcorn Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA
Package size9.75 oz
UPC843571000693, 843571001676

FDA code information

9.75 oz. 12223ENGA 2/6/2013 14 oz. 12223ENGA 2/6/2013 0.7 Oz 12221ENGA 2/4/2013

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Full FDA record and distribution details

Original product description

Popcorn Indiana Kettlecorn Net Wt. 9.75 oz UPC 84357100050 Net Wt. 14 oz. UPC 843571000693 Net Wt. 8 pack bag 0.7 oz. UPC 843571001676 Popcorn Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA

Extracted codes and context

TypeCode / valueContext
UPC843571000693Popcorn Indiana Kettlecorn Net Wt. 9.75 oz UPC 84357100050 Net Wt. 14 oz. UPC 843571000693 Net Wt. 8 pack bag 0.7 oz. UPC 843571001676 Popcorn Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA
UPC843571001676PC 84357100050 Net Wt. 14 oz. UPC 843571000693 Net Wt. 8 pack bag 0.7 oz. UPC 843571001676 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-0591-2013
Event ID
63303
FDA status
Terminated
Initiated
Sep 18, 2012
Reported
Nov 7, 2012
Classified
Nov 1, 2012
Terminated
Sep 25, 2013
Quantity
83,256 bags
Location
Englewood, NJ, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide, Canada

FDA source record · F-0591-2013

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

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