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Class IITerminated in FDA datasetRecall initiated Sep 18, 2012

Popcorn Indiana Chocolate Peanut Butter Kettlecorn Net Wt 5 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.

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

ProductPopcorn Indiana Chocolate Peanut Butter Kettlecorn Net Wt 5 oz. UPC 843571003786 Net Wt. 5.5 oz UPC 843571003847 Popcorn Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA
Package size5 oz
UPC843571003786, 843571003847

FDA code information

12222ENGA 2/5/2013 12251ENGA 3/6/2013 12240ENGA 2/23/2013 12241ENGA 2/24/2013 12237ENGA 2/20/2013

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 Chocolate Peanut Butter Kettlecorn Net Wt 5 oz. UPC 843571003786 Net Wt. 5.5 oz UPC 843571003847 Popcorn Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA

Extracted codes and context

TypeCode / valueContext
UPC843571003786Popcorn Indiana Chocolate Peanut Butter Kettlecorn Net Wt 5 oz. UPC 843571003786 Net Wt. 5.5 oz UPC 843571003847 Popcorn Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA
UPC843571003847te Peanut Butter Kettlecorn Net Wt 5 oz. UPC 843571003786 Net Wt. 5.5 oz UPC 843571003847 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-0589-2013
Event ID
63303
FDA status
Terminated
Initiated
Sep 18, 2012
Reported
Nov 7, 2012
Classified
Nov 1, 2012
Terminated
Sep 25, 2013
Quantity
18,798 units
Location
Englewood, NJ, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Nationwide, Canada

FDA source record · F-0589-2013

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

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