NGMO Ballard Semisweet Chocolate Wafer, Item # 59343. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Choc
Summary
The FDA issued a Class III for NGMO Ballard Semisweet Chocolate Wafer, Item # 59343. Net Wt. 50 lbs. (22.68 KG by Clasen Quality Chocolater, Inc. Reason: Chocolate may contain undeclared peanut residue..
Details
Source
Food Recall
External ID
F-0443-2023
Action Date
2023-03-22
Status
Terminated
Category
food
Product Description
NGMO Ballard Semisweet Chocolate Wafer, Item # 59343. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Chocolate Liquor (Processed with Alkali), Sugar, Cocoa Butter, Butterfat (Milk), Sunflower Lecithin (an emulsifier), Vanilla Extract. Distributed By: Clasen Quality Chocolate, 5126 West Terrace Drive, Madison, WI 53718
Lot/Code Info: Lot # 2309CH51CL15, 2353CH44CL15.
Quantity Affected: 77,850 lbs.
Reason for Recall
Chocolate may contain undeclared peanut residue.
Distribution
CA, CO, IL, KY, MA, MI, NJ, NY, OR, PA, UT, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2023-01-18
Company
Watertown, WI
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 488 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Clasen Quality Chocolater, Inc has 18 FDA actions in our database, including 18 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 (Clasen Quality Chocolater, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Clasen Quality Chocolater, Inc have FDA actions?
Clasen Quality Chocolater, Inc has 18 FDA actions in our database, including 18 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0443-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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