CLASS I Food recall · Reported 20 Jul 2022 · FDA Enforcement Report

Favorite Day Lavender Shortbread Cookie Bites recalled by J & M Foods

J & M Foods is recalling Favorite Day Lavender Shortbread Cookie Bites, distributed in 18 states. The recall was initiated on 16 Jun 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest Before 18.Apr.2023

Quantity recalled244 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-1414-2022
FDA event ID: 90461
Recalling firm: J & M Foods, Little Rock, AR
Brand: Favorite Day
Classification: Class I
Status: Terminated
Recall initiated: 16 Jun 2022
FDA classified: 13 Jul 2022
Reported: 20 Jul 2022
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Undeclared Egg
Product category: Cookies

Timeline

16 Jun 2022	Recall initiated by company
13 Jul 2022	Classified by FDA	+27 days
20 Jul 2022	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Undeclared egg and soy lecithin

Product as listed by the FDA

Favorite Day Lavender Shortbread Cookie Bites Net Wt 7oz (198g) packaged in a purple bag and an inside silver flexible bag UPC 085239286098, 6 units per case

Where it was distributed

SC, OH, TX, KS, GA, CA, NC, WI, MI, AL, VA, NY, NJ, IL, MN, CO, OR, IN

Alabama California Colorado Georgia Illinois Indiana Kansas Michigan Minnesota North Carolina New Jersey New York Ohio Oregon South Carolina Texas Virginia Wisconsin

Stores named: Target

Questions about this recall

Why was it recalled?

Undeclared egg and soy lecithin

Which lots are affected?

Best Before 18.Apr.2023

Where was it sold?

SC, OH, TX, KS, GA, CA, NC, WI, MI, AL, VA, NY, NJ, IL, MN, CO, OR, IN

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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