Class IIITerminatedVoluntary: Firm initiated
D.F.S. International, Ltd.: food recall H-0253-2025
D.F.S. International, Ltd. of Springfield, MA recalled Daniele brand First Cold Press EXTRA VIRGIN OLIVE OIL; NET 101.4 FL. OZ. (3 QT. 5.4 FL. OZ.) 3L; IMPORTED; Distributed… Reason: Product is likely Canola Oil, not Extra Virgin Olive Oil. The FDA listed it as Class III in its Enforcement Report dated Jul 16, 2025; distribution: New York.
Record status as published: Terminated (terminated Sep 26, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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
- Product quantity
- 10 cases
- Reason for recall
- Product is likely Canola Oil, not Extra Virgin Olive Oil
- Codes, lots and dates on the package
- BEST BY 08/08/26 Lot # 4221
- Distribution pattern
- NY
- Recalling firm
- D.F.S. International, Ltd., Springfield, MA
- Classification
- Class III — the FDA uses this class for a situation in which using or being exposed to the product is not likely to cause adverse health consequences.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Letter
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jan 6, 2025 |
| Classified by the FDA | Jul 10, 2025 |
| Published in the Enforcement Report | Jul 16, 2025 |
| Terminated | Sep 26, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0253-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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