Aged White Cheddar 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 Aged White Cheddar Popcorn 0.8 oz - UPC 843571004233 3.5 oz- UPC 843571000532 8 oz- UPC 843571000785 8.3 oz - UPC 843571002956 9 oz - UPC843571000785 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
3.5 oz 12228ENGA 2/11/2013 12233ENGA 2/16/2013 12242ENGA 2/25/2013 12244ENGA 2/27/2013 12254ENGA 3/9/2013 12255ENGA 3/10/2013 8 oz. 12222ENGA 2/5/2013 12228ENGA 2/11/2013 12235ENGA 2/18/2013 12243ENGA 2/26/2013 12244ENGA 2/27/2013 12254ENGA 3/9/2013 12255ENGA 3/10/2013 8.3 oz 12222ENGA 2/5/2013 12235ENGA 2/18/2013 12242ENGA 2/25/2013 12244ENGA 2/27/2013 Canada 9.3 oz. 12235ENGA 2/18/2013 12242ENGA 2/25/2013
Dale & Thomas Popcorn, LLC is recalling Popcorn Indiana Aged White Cheddar Popcorn 0.8 oz - UPC 843571004233 3.5 oz- UPC 843571000532 8 oz due to Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono. This recall was expanded to the consumer level onc. 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. This recall was expanded to the consumer level once L. mono was confirmed in finished product.
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