Datil del Oasis de Mexico, S.A. de C.V.
FDA import alert and refusal historyMexicali, MexicoFEI 3032732040
As of October 26, 2026, Datil del Oasis de Mexico, S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between January 28, 2026 and October 1, 2026, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Dates (pit fruit), (pit fruit) · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Datil del Oasis de Mexico, S.A. de C.V.
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY2 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Datil del Oasis de Mexico, S.A. de C.V.
- Is Datil del Oasis de Mexico, S.A. de C.V. on an FDA import alert?
- No listing for Datil del Oasis de Mexico, S.A. de C.V. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
- Has FDA refused shipments from Datil del Oasis de Mexico, S.A. de C.V.?
- Yes. FDA refused 2 shipment lines from Datil del Oasis de Mexico, S.A. de C.V. between January 28, 2026 and October 1, 2026. The most recent, on October 1, 2026, was dates (pit fruit), (pit fruit), charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Datil del Oasis de Mexico, S.A. de C.V.'s shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
- What is Datil del Oasis de Mexico, S.A. de C.V.'s FEI number?
- Datil del Oasis de Mexico, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3032732040.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.