FDA recall record

Dale & Thomas Popcorn Popcorn Indiana Kettlecorn Net Wt recall — FDA F-0591-2013

Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.

Class IIclassification
F-0591-2013official record ID
Nov 7, 2012report date

Recall record at a glance

Official recordF-0591-2013
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmDale & Thomas Popcorn, LLC
Report dateNov 7, 2012
Recall initiation dateSep 18, 2012
Quantity83,256 bags
LocationEnglewood, NJ, United States

Official product description

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

Why the product was recalled

Various flavors of popcorn were manufactured on a conveyor belt which tested positive for L. mono.

Distribution information

Nationwide, Canada

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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