Daniele brand First Cold Press EXTRA VIRGIN OLIVE OIL; NET 101.4 FL. OZ. (3 QT. 5.4 FL. OZ.) 3L; IMPORTED; Distributed b
Summary
The FDA issued a Class III for Daniele brand First Cold Press EXTRA VIRGIN OLIVE OIL; NET 101.4 FL. OZ. (3 QT. by D.F.S. International, Ltd.. Reason: Product is likely Canola Oil, not Extra Virgin Olive Oil.
Details
Source
Food Recall
External ID
H-0253-2025
Action Date
2025-07-16
Status
Terminated
Category
food
Product Description
Daniele brand First Cold Press EXTRA VIRGIN OLIVE OIL; NET 101.4 FL. OZ. (3 QT. 5.4 FL. OZ.) 3L; IMPORTED; Distributed by: dfs international ltd Springfield, ma 01104; INGREDIENTS: EXTRA VIRGIN OLIVE OIL; Product contains select high quality Extra Virgin Olive Oil from the countries: I=Italy, E=Spain, GR=Greece; TN=Tunisia; UPC: 036821110116
Lot/Code Info: BEST BY 08/08/26 Lot # 4221
Quantity Affected: 10 cases
Reason for Recall
Product is likely Canola Oil, not Extra Virgin Olive Oil
Distribution
NY
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-06
Company
Springfield, MA
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 147 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 (D.F.S. International, Ltd.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does D.F.S. International, Ltd. have FDA actions?
This is the only FDA action we have on record for D.F.S. International, Ltd. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0253-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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