ERIDANOUS GREEK STYLE Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling. Product is packed onto a plas
Summary
The FDA issued a Class II for ERIDANOUS GREEK STYLE Shortbread Cookies with Chocolate Truffle Coating & Aprico by Lidl US TRADING. Reason: The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy,.
Details
Source
Food Recall
External ID
H-1274-2026
Action Date
2026-09-02
Status
Ongoing
Category
food
Product Description
ERIDANOUS GREEK STYLE Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling. Product is packed onto a plastic carton tray with outer paper sleeve, 330 g (weight), UPC: 4056489125839.
Lot/Code Info: BEST BEFORE: 10/11/2026 LOT NO: 260315
Quantity Affected: 500 units
Reason for Recall
The firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coconut).
Distribution
Product was shipped to the following states: DC, DE, GA, MD, NJ, NY, NC, PA, SC, & VA.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-07-22
Company
Arlington, VA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 47 food recalls issued in the same week, part of 82 food-related FDA actions this month.
Lidl US TRADING has 18 FDA actions in our database, including 18 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Lidl US TRADING) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lidl US TRADING have FDA actions?
Lidl US TRADING 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 "H-1274-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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