Popcorn Indiana Bacon Ranch Popcorn Net Wt. 3.5 oz -
Recalling firm: Dale & Thomas Popcorn, LLC
Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 25, 2013.
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843571001935, 843571001942FDA code information
6 count 3.5 oz. 12235ENGA 2/18/2013 12251ENGA 3/6/2013 12254ENGA 3/9/2013 12255ENGA 3/10/2013 6 count 8.3 oz 12229ENGA 2/12/2013 12235ENGA 2/18/2013 12251ENGA 3/6/2013 12 count 7.75 oz. 12235ENGA 2/18/2013
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Full FDA record and distribution details
Original product description
Popcorn Indiana Bacon Ranch Popcorn Net Wt. 3.5 oz - UPC 843571001942 Net Wt. 7.75 oz - UPC 843571001935 Net Wt. 8.3oz. - UPC 843571001935 Popcorn, Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 843571001935 | a Bacon Ranch Popcorn Net Wt. 3.5 oz - UPC 843571001942 Net Wt. 7.75 oz - UPC 843571001935 Net Wt. 8.3oz. - UPC 843571001935 Popcorn, Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA |
| UPC | 843571001935 | oz - UPC 843571001942 Net Wt. 7.75 oz - UPC 843571001935 Net Wt. 8.3oz. - UPC 843571001935 Popcorn, Indiana LLC 1 Cedar Lane, Englewood, NJ 07631 Made in the USA |
| UPC | 843571001942 | Popcorn Indiana Bacon Ranch Popcorn Net Wt. 3.5 oz - UPC 843571001942 Net Wt. 7.75 oz - UPC 843571001935 Net Wt. 8.3oz. - UPC 843571001935 Popcorn, Indiana LLC 1 Cedar Lane, Englewood, N |
Original FDA recall reason
Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.
Recall details
- Recall number
- F-0581-2013
- Event ID
- 63303
- FDA status
- Terminated
- Initiated
- Sep 18, 2012
- Reported
- Nov 7, 2012
- Classified
- Nov 1, 2012
- Terminated
- Sep 25, 2013
- Quantity
- 36,246 units
- Location
- Englewood, NJ, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
Nationwide, Canada
Data updated September 16, 2026. View official FDA data ↗
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