CLASS III Food recall · Reported 16 Jul 2025 · FDA Enforcement Report
Daniele First Cold Press Extra Virgin Olive Oil recalled
D.F.S. International is recalling Daniele First Cold Press Extra Virgin Olive Oil, distributed in New York. The recall was initiated on 6 Jan 2025 and the FDA has classified it as Class III.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0253-2025
- FDA event ID
- 97004
- Recalling firm
- D.F.S. International, Springfield, MA
- Brand
- Daniele
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- 6 Jan 2025
- FDA classified
- 10 Jul 2025
- Reported
- 16 Jul 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Product category
- Cooking Oil
Timeline
| 6 Jan 2025 | Recall initiated by company | |
| 10 Jul 2025 | Classified by FDA | +185 days |
| 16 Jul 2025 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product is likely Canola Oil, not Extra Virgin Olive Oil
Product as listed by the FDA
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
Where it was distributed
NY
Questions about this recall
Why was it recalled?
Product is likely Canola Oil, not Extra Virgin Olive Oil
Which lots are affected?
BEST BY 08/08/26 Lot # 4221
Where was it sold?
NY
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class III mean?
Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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