Dill Pickle Lite Works Popcorn
Reason The product contains an allergen that is not declared on the label (Milk)
Candy coated popcorn shaped into a heart weighing 1.5 ounces per… recall
Recalled by Popcorn Factory, The · Lake Forest, IL, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The Nutrition Facts and allergen label was not applied individual popcorn balls in a Valentine's Day promotion package. The popcorn balls contain milk and soy allergens.
Undeclared allergens: Milk Soy
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Candy coated popcorn shaped into a heart weighing 1.5 ounces per piece and individually wrapped in clear plastic packaging. There are 24 popcorn balls per case.
Quantity: 27 cases (648 popcorn balls)
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.
Product Lot Number: 14022. Case Lot Number: 14034. Expiration Date: April 7, 2014.
Where it was sold
Nationwide.
California Connecticut Florida Georgia Illinois Kansas Michigan New Jersey New Mexico Nevada New York Ohio Pennsylvania Texas Vermont Wisconsin
FDA's distribution note: US: Nationwide (CA, CT, FL, GA, IL, KS, MI, NJ, NM, NV, NY, OH, PA, TX, VT ,WI)
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. The risk from an undeclared allergen is to people allergic to milk, soy; for anyone else the product is generally not a safety concern. 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
- Popcorn Factory, The
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 4, 2014
- In FDA report of
- Mar 5, 2014
- Terminated
- Mar 28, 2016
- FDA recall number
- F-1553-2014 · event 67467
- Official record
- FDA enforcement report search
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