Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 23, 2022 (4 years ago)

Avery's Savory Popcorn Gourmet Popcorn All Flavors packaged in… recall

Recalled by Averys Savory Popcorn, LLC · Dallas, TX, United States

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

Why it was recalled

The recalled product contains undeclared milk, soy, peanuts, tree nuts (almonds, walnuts, pecans, cashews), and sulfites

Undeclared allergens: Milk Peanut Tree nuts 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

Avery's Savory Popcorn Gourmet Popcorn All Flavors packaged in clear plastic flexible bags heat sealed, unit size 1.5 cups to 26 cups

Quantity: 3185 units

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.

shipped to consumers between November 20, 2022, and December 20, 2022

Where it was sold

Connecticut Florida Georgia Kentucky Maryland Ohio Oklahoma Rhode Island Texas

FDA's distribution note: Connecticut, Florida, Georgia, Kentucky, Maryland, Ohio, Oklahoma, Rhode Island, and Texas.

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, peanut, tree nuts, 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
Averys Savory Popcorn, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 23, 2022
In FDA report of
Feb 1, 2023
Terminated
Feb 10, 2023
FDA recall number
F-0309-2023 · event 91444
Official record
FDA enforcement report search

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