Kilwin's Mocha Truffle bulk 2.5lbs Kilwin's Mocha Truffles 4.75oz UPC 0 043110 5
Summary
The FDA issued a Class I for Kilwin's Mocha Truffle bulk 2.5lbs Kilwin's Mocha Truffles 4.75oz UPC 0 043110 5 by Kilwin's Quality Confections, Inc.. Reason: undeclared pecans.
Details
Source
Food Recall
External ID
H-0281-2025
Action Date
2025-07-23
Status
Terminated
Category
food
Product Description
Kilwin's Mocha Truffle bulk 2.5lbs Kilwin's Mocha Truffles 4.75oz UPC 0 043110 5
Lot/Code Info: Batch Code B156786 (bulk unit). None on retail unit.
Quantity Affected: 130 lbs total across all recalled products
Reason for Recall
undeclared pecans
Distribution
NC, FL, MD, DE, MI, NH, IL, VA, OH, GA, AL, DC, TX, LA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-05-27
Company
Petoskey, MI
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 98 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Kilwin's Quality Confections, Inc. has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Kilwin's Quality Confections, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kilwin's Quality Confections, Inc. have FDA actions?
Kilwin's Quality Confections, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0281-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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