Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 29, 2023 (4 years ago)

Cookies con Amore handmade italian cookies Spring Assortment recall

Recalled by Con Amore, Inc · San Marcos, CA, United States

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

Why it was recalled

Undeclared allergen; tree nuts (almonds)

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

Cookies con Amore handmade italian cookies Spring Assortment 32 oz (907g) Contains Allergens: Wheat, Dairy, Egg This product is produced in a facility that uses wheat, sesame seeds, and a variety of tree nuts. www.cookiesconamore.com Con Amore, Inc. San Marcos, CA UPC 8 92886 00096 6

Quantity: 34,560 units

Food: Bread & bakery

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.

Best by Dates: 9/3/23, 9/4/23, 9/5/23, 9/6/23, 9/9/23, 9/10/23, 9/11/23, 9/12/23, 9/13/23, 9/16/23, 9/17/23, 9/18/23

Where it was sold

Arizona California Colorado

FDA's distribution note: U.S. distribution to: CA, CO, AZ

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
Con Amore, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 29, 2023
In FDA report of
May 3, 2023
Terminated
Jun 9, 2023
FDA recall number
F-0768-2023 · event 92010
Official record
FDA enforcement report search

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