Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 10, 2022 (5 years ago)

Favorite Day Carrot cake soft bake cookies recall

Recalled by J & M Foods, Inc. · Little Rock, AR, United States

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

Why it was recalled

Pecans although listed in the Ingredient Statement, was omitted from the CONTAINS statement.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

Favorite Day Carrot cake soft bake cookies Net Wt 8 oz. (227g) UPC 0 885239 25803 3 packaged in gable top carton 6 units per case

Quantity: 9309 cases

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 Before: 07-OCT-2022, 08-OCT-2022, 09-OCT-2022 & 10-OCT-2022; Lots: 22010FDSBCC86, 22011FDSBCC86, 21012FDSBCC86, 22013FDSBCC86

Where it was sold

Alabama Arizona California Colorado Connecticut District of Columbia Florida Georgia Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Maine Michigan Minnesota Missouri Mississippi North Carolina New Hampshire New Jersey New Mexico New York Ohio Oregon Pennsylvania South Carolina Texas Utah Virginia Vermont Washington Wisconsin

FDA's distribution note: AL, AZ, CA, CO, CT, DC, FL, GA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NH, NJ, NM, NY, OH, OR, PA, SC, TX, UT, VA, VT, WA, WI

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. 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
J & M Foods, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 10, 2022
In FDA report of
Mar 9, 2022
Terminated
Apr 12, 2024
FDA recall number
F-0804-2022 · event 89593
Official record
FDA enforcement report search

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