Food Recall Check
Class II · Moderate risk Terminated Initiated Apr 9, 2022 (4 years ago)

12/5 oz bags of O-Organic Sea Salt Popcorn recall

Recalled by Snak King Corporation · City Of Industry, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

A potato stick snack with a milk allergen was found in the O-Organic Sea Salt Popcorn line's recycle chute.

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

12/5 oz. bags of O-Organic Sea Salt Popcorn. UPC Code: 79893403038

Quantity: 4832 cases

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 numbers: 8124905, 80125929, 8125929, 8124905, 8125929 ; Best buy dates 09/24/2022 and 09/25/2022.

Where it was sold

Alaska California Connecticut District of Columbia Delaware Hawaii Iowa Idaho Illinois Indiana Maryland New Jersey Nevada New York Oregon Pennsylvania Virginia Washington

FDA's distribution note: Connecticut, Delaware, Maryland, New Jersey, New York, Pennsylvania, Virginia, Washington DC, Illinois, Indiana, Iowa, California, Hawaii, Nevada, Oregon, Washington, Alaska, and Idaho.

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; 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
Snak King Corporation
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 9, 2022
In FDA report of
May 18, 2022
Terminated
Jun 30, 2022
FDA recall number
F-1050-2022 · event 89985
Official record
FDA enforcement report search

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