RecallHawk
Class I Recall

Kilwin's Truffle Assortment 9.5oz UPC 0 004574 0 Kilwin's Truffle Assortment 8oz UPC 0 043109 5 Kilwin's Truffle Assortm

Kilwin's Quality Confections, Inc.

Summary

The FDA issued a Class I for Kilwin's Truffle Assortment 9.5oz UPC 0 004574 0 Kilwin's Truffle Assortment 8oz by Kilwin's Quality Confections, Inc.. Reason: undeclared pecans.

Details

Source

Food Recall

External ID

H-0282-2025

Action Date

2025-07-23

Status

Terminated

Category

food

Product Description

Kilwin's Truffle Assortment 9.5oz UPC 0 004574 0 Kilwin's Truffle Assortment 8oz UPC 0 043109 5 Kilwin's Truffle Assortment 4.75oz UPC 0 044121 8

Lot/Code Info: None

Quantity Affected: 130lbs 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

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-0282-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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