Drizzilicious Mini Rice Cake bites Net Wt.4oz and or .74oz Bags Cinnamon Swirl UPC: 857900005167 and UPC:857900005181 P
Summary
The FDA issued a Class III for Drizzilicious Mini Rice Cake bites Net Wt.4oz and or .74oz Bags Cinnamon Swirl by Snack Innovations Inc.. Reason: May contain undeclared peanut residue..
Details
Source
Food Recall
External ID
F-0393-2023
Action Date
2023-03-08
Status
Terminated
Category
food
Product Description
Drizzilicious Mini Rice Cake bites Net Wt.4oz and or .74oz Bags Cinnamon Swirl UPC: 857900005167 and UPC:857900005181 Packaged in a plastic bags Product also packed in the Drizzilicious mini rice cakes 32-ct Variety box
Lot/Code Info: Best By 22 SEP2023 N3-11BHNV3562 Best By 16OCT2023 N4-11BHNV0163 Best By 05OCT2023 N3-11BHNV0053 Best By 22SEP2023 N4-11BHNV3562 Best By 19SEP2023 N4-21BHNV3532
Quantity Affected: 10429
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-0393-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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