Caramel Popcorn (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 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
Brand
Dale & Thomas Popcorn, LLC
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
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
Dale & Thomas Popcorn, LLC is recalling Popcorn Indiana Caramel Popcorn Net Wt. 7.4 oz. UPC 843571003045 Net Wt. 8 oz - UPC 843571002369 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 12, 2026