Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 2, 2020 (7 years ago)

purely elizabeth Chocolate Sea Salt probiotic granola recall

Recalled by purely elizabeth. · Boulder, CO, United States

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

Why it was recalled

Undeclared Walnut Allergen. Maple Walnut Probiotic granola was packaged in Chocolate Sea Salt probiotic granola bags.

Undeclared allergen: Tree nuts

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

purely elizabeth Chocolate Sea Salt probiotic granola. Net Wt. 8 oz (227g). UPC 55140-00268. Made with organic quinoa, amaranth and chia. Contains Coconut. May contain Walnuts, Cashews and Almonds. Made in a facility that also processes soy, milk, eggs, peanuts and other tree nuts.

Quantity: 3,719 cases (6 units per case) total

Food: Chocolate & candy Pasta, rice & grains

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: OH29519 / Best By: 10/21/2020

Where it was sold

Illinois

FDA's distribution note: IL

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 tree nuts; 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
purely elizabeth.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 2, 2020
In FDA report of
Jan 15, 2020
Terminated
Aug 16, 2021
FDA recall number
F-0499-2020 · event 84613
Official record
FDA enforcement report search

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