Kettlecorn (Dale & Thomas) – listeria contamination (2012)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
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
Brand
Dale & Thomas Popcorn, LLC
Lot Codes / Batch Numbers
9.75 oz. 12223ENGA 2/6/2013 14 oz. 12223ENGA 2/6/2013 0.7 Oz 12221ENGA 2/4/2013
Products Sold
9.75 oz. 12223ENGA 2/6/2013 14 oz. 12223ENGA 2/6/2013 0.7 Oz 12221ENGA 2/4/2013
Dale & Thomas Popcorn, LLC is recalling Popcorn Indiana Kettlecorn Net Wt. 9.75 oz UPC 84357100050 Net Wt. 14 oz. UPC 843571000693 Net Wt due to Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 13, 2026