The Recall Desk
HighFDA (Food)·F-0583-2013·Announced 2012-11-07

Popcorn Indiana Drizzled Cinnamon Sugar Kettlecorn Recalled for Listeria

Dale & Thomas Popcorn, LLC is recalling Popcorn Indiana Drizzled Cinnamon Sugar Kettlecorn because the manufacturing conveyor belt tested positive for Listeria monocytogenes.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a high-risk pathogen (Listeria monocytogenes) without reported illnesses, which meets the criteria for a High severity score.

Plain-English summary

Dale & Thomas Popcorn, LLC is recalling 192 units of Popcorn Indiana Drizzled Cinnamon Sugar Kettlecorn. The affected products are the 5.5 oz. (UPC 843571003052) and 6 oz. (UPC 843571002352) varieties. The recall covers specific production codes: 12255ENGA (3/10/2013), 12236ENGA (2/19/2013), and 12241ENGA (2/24/2013).

The recall was initiated because the popcorn was manufactured on a conveyor belt that tested positive for Listeria monocytogenes (L. mono). The products were distributed nationwide and in Canada.

Consumers who have purchased these specific products should check their pantry for the listed UPCs and production codes. If the products are found, they should be discarded or returned to the place of purchase.

The recalled product

Product
Popcorn Indiana Drizzled Cinnamon Sugar Kettlecorn Net Wt. 5.5 oz. UPC 843571003052 Net Wt. 6 oz UPC 843571002352 Popcorn Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA
Hazard
Affected units
192

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • 6 oz. 12255ENGA 3/10/2013 12236ENGA 2/19/2013 12241ENGA 2/24/2013

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 14 recalled by Dale & Thomas Popcorn, LLC under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 14 products in this recall →