Daniele brand First Cold Press EXTRA VIRGIN OLIVE OIL; NET 101.4 FL. OZ. (3 QT. 5.4 FL.
D.F.S. International, Ltd. recalled this product and the FDA reported the enforcement action on 16 July 2025 as Class III. The recall was initiated by the firm. Product is likely Canola Oil, not Extra Virgin Olive Oil
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- 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
- UPC
- 036821110116
- Reason for recall
- Product is likely Canola Oil, not Extra Virgin Olive Oil
- Recalling firm
- D.F.S. International, Ltd.
- Firm location
- Springfield, Massachusetts, United States
- Classification
- Class III
- Status
- Terminated
- Recall number
- H-0253-2025
- Quantity
- 10 cases
- Distribution
- NY
- Initiated
- 6 January 2025
- Reported by FDA
- 16 July 2025
- Terminated
- 26 September 2025
- Firm notified by
- Letter
- Product codes
- BEST BY 08/08/26 Lot # 4221
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class III means the FDA judged that the product was unlikely to cause harm but violated FDA labelling or manufacturing regulation. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This record is the only one the FDA opened for its recall event, so it covers a single product code.
- The recall ran for 9 months, from 6 January 2025 to termination on 26 September 2025. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The distribution pattern names 1 state, and the FDA published the enforcement report 6 months after the firm began the recall.
- The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.
All 2025 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.