chuao CHOCOLATIER potato chip mini chocolate bar, 0.39oz/11g
Summary
The FDA issued a Class III for chuao CHOCOLATIER potato chip mini chocolate bar, 0.39oz/11g by Kairo's Group, Inc. dba Chuao Chocolatier. Reason: Undeclared hazelnut.
Details
Source
Food Recall
External ID
F-1420-2024
Action Date
2024-05-29
Status
Terminated
Category
food
Product Description
chuao CHOCOLATIER potato chip mini chocolate bar, 0.39oz/11g
Lot/Code Info: LOT 4022, Best by 22 FEB 25
Quantity Affected: 13,312 bars
Reason for Recall
Undeclared hazelnut
Distribution
U.S. distribution to distributors, retailers, and consumers in the following states: AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI. Foreign distribution to 4 consumers in Japan, England, Singapore, and Indonesia.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-05-03
Company
Carlsbad, CA
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 27 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Kairo's Group, Inc. dba Chuao Chocolatier) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kairo's Group, Inc. dba Chuao Chocolatier have FDA actions?
This is the only FDA action we have on record for Kairo's Group, Inc. dba Chuao Chocolatier in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1420-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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