Snack Day by Lidl Vanilla Flavored Kettle Corn Drizzled with Rainbow Sprinkles Net Wt. 5 oz (141g) Packaged in a plast
Summary
The FDA issued a Class III for Snack Day by Lidl Vanilla Flavored Kettle Corn Drizzled with Rainbow Sprinkles by Snack Innovations Inc.. Reason: May contain undeclared peanut residue..
Details
Source
Food Recall
External ID
F-0399-2023
Action Date
2023-03-08
Status
Terminated
Category
food
Product Description
Snack Day by Lidl Vanilla Flavored Kettle Corn Drizzled with Rainbow Sprinkles Net Wt. 5 oz (141g) Packaged in a plastic bags.
Lot/Code Info: N4-11BHNV3552 8/21/2023 240341002
Quantity Affected: 1660 cases
Reason for Recall
May contain undeclared peanut residue.
Distribution
Distributed to distributors in OH, CT, CA, TX, MA, FL, NY, CO, RI, WA in the US.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-01-20
Company
Piscataway, NJ
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 45 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Snack Innovations Inc. has 8 FDA actions in our database, including 8 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
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 (Snack Innovations Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Snack Innovations Inc. have FDA actions?
Snack Innovations Inc. has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0399-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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