Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. UPC 000011 812722. Product is packaged i
Summary
The FDA issued a Class I for Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. by Costco Wholesale Corporation. Reason: Undeclared hazelnut..
Details
Source
Food Recall
External ID
H-0491-2026
Action Date
2026-02-18
Status
Terminated
Category
food
Product Description
Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. UPC 000011 812722. Product is packaged in a clear clamshell container. ALLERGENS INFORMATION: CONTAINS WHEAT, EGG, MILK, SOY. Distributed by Costco Wholesale Corp. PO Box 34535 Seattle, WA.
Lot/Code Info: Pack Dates: Jan 16, 26 - Jan 30, 26 Sell by Dates: Jan 19, 26 - Feb 2, 26
Quantity Affected: 8073 packages
Reason for Recall
Undeclared hazelnut.
Distribution
Distributed in Alabama, Arizona, California, Colorado, Florida, Georgia, Hawaii, Idaho, Illinois, Iowa, Louisiana, Michigan, Missouri, Nevada, New Jersey, New York, Ohio, Oregon, Pennsylvania, South Dakota, Tennessee, Texas, Virginia, and Washington.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-01-31
Company
Issaquah, WA
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 70 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Costco Wholesale Corporation has 5 FDA actions in our database, including 5 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 (Costco Wholesale Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Costco Wholesale Corporation have FDA actions?
Costco Wholesale Corporation has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0491-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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