Popcorn Indiana Bacon Ranch Popcorn
Reason Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Popcorn Indiana Aged White Cheddar Popcorn recall
Recalled by Dale & Thomas Popcorn, LLC · Englewood, NJ, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
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.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
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
Quantity: 398910 bags
Food: Cheese Chips & snacks
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
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
Where it was sold
Nationwide.
FDA's distribution note: Nationwide, Canada
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Dale & Thomas Popcorn, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 18, 2012
- In FDA report of
- Nov 7, 2012
- Terminated
- Sep 25, 2013
- FDA recall number
- F-0580-2013 · event 63303
- Official record
- FDA enforcement report search
Also recalled with it (13 more products)
FDA files each product of one recall action separately; these share the same FDA event.
Popcorn Indiana American Cheese Popcorn
Reason Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Popcorn Indiana Drizzled Cinnamon Sugar Kettlecorn
Reason Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Popcorn Indiana Almond Biscotti Caramel Popcorn
Reason Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Popcorn Indiana Apple Crisp Popcorn
Reason Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Popcorn Indiana Drizzled Black & White Kettlecorn
Reason Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Popcorn Indiana Caramel Popcorn
Reason Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Popcorn Indiana Roasted Peanut Caramel Popcorn
Reason Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Popcorn Indiana Chocolate Peanut Butter Kettlecorn
Reason Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Popcorn Indiana Dark Fudge Chocolate Chip Kettlecorn
Reason Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Popcorn Indiana Kettlecorn
Reason Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Popcorn Indiana Salt and Pepper Popcorn
Reason Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
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