Milk & Dark Chocolate Caramel Macchiato. Chocolate coated caramels packaged in bulk and distributed in bulk to the firm
Summary
The FDA issued a Class III for Milk & Dark Chocolate Caramel Macchiato. Chocolate coated caramels packaged in by R & S Roberts Enterprises, Inc.. Reason: Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin..
Details
Source
Food Recall
External ID
F-1064-2022
Action Date
2022-05-25
Status
Terminated
Category
food
Product Description
Milk & Dark Chocolate Caramel Macchiato. Chocolate coated caramels packaged in bulk and distributed in bulk to the firm's stores in a bin. UPC 7 82565 11777 4.
Lot/Code Info: Manufacture date: 03/22/2022 Tracking By Manufacture Date: 03/22/2022
Quantity Affected: 48 pieces
Reason for Recall
Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.
Distribution
Distributed in Washington.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-04-27
Company
Auburn, WA
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 25 food recalls issued in the same week, part of 204 food-related FDA actions this month.
R & S Roberts Enterprises, Inc. has 6 FDA actions in our database, including 6 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 (R & S Roberts Enterprises, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does R & S Roberts Enterprises, Inc. have FDA actions?
R & S Roberts Enterprises, Inc. has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1064-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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