Candy coated popcorn shaped into a heart weighing 1.5 ounces per…
Reason 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.
Dill Pickle Lite Works Popcorn recall
Recalled by Popcorn Factory, The · Lake Forest, IL, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The product contains an allergen that is not declared on the label (Milk)
Undeclared allergen: Milk
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
Dill Pickle Lite Works Popcorn , lot number 15111, packaged in a 4 oz foil white bag with black and green lettering.
Quantity: 600, 4 oz bags
Food: 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.
Lot code 15111, Best by date SEP 17, 2015
Where it was sold
New Jersey
FDA's distribution note: US: NJ
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; 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
- May 27, 2015
- In FDA report of
- Jul 15, 2015
- Terminated
- Mar 30, 2017
- FDA recall number
- F-2818-2015 · event 71358
- Official record
- FDA enforcement report search
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