Favorite Day Lavender Shortbread Cookie Bites Net Wt 7oz (198g) packaged in a purple bag and an inside silver flexible
Summary
The FDA issued a Class I for Favorite Day Lavender Shortbread Cookie Bites Net Wt 7oz (198g) packaged in a p by J & M Foods, Inc.. Reason: Undeclared egg and soy lecithin.
Details
Source
Food Recall
External ID
F-1414-2022
Action Date
2022-07-20
Status
Terminated
Category
food
Product Description
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
Lot/Code Info: Best Before 18.Apr.2023
Quantity Affected: 244 cases
Reason for Recall
Undeclared egg and soy lecithin
Distribution
SC, OH, TX, KS, GA, CA, NC, WI, MI, AL, VA, NY, NJ, IL, MN, CO, OR, IN
Type: Voluntary: Firm initiated
Recall Initiated: 2022-06-16
Company
Little Rock, AR
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 41 food recalls issued in the same week, part of 204 food-related FDA actions this month.
J & M Foods, Inc. has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (J & M Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does J & M Foods, Inc. have FDA actions?
J & M Foods, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1414-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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