Harvest Tek de Mexico Spr de Rlde CV
FDA import alert and refusal historyMexicali, MexicoFEI 3014537000
Recorded by FDA as HARVEST TEK DE MEXICO SPR DE RLDE CV
As of October 26, 2026, Harvest Tek de Mexico Spr de Rlde CV is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between August 25, 2025 and October 16, 2025, most often for pesticide chemical residue (PESTICIDE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Grass hay · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Harvest Tek de Mexico Spr de Rlde CV
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE3 refused lines
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about Harvest Tek de Mexico Spr de Rlde CV
- Is Harvest Tek de Mexico Spr de Rlde CV on an FDA import alert?
- No listing for Harvest Tek de Mexico Spr de Rlde CV 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 Harvest Tek de Mexico Spr de Rlde CV?
- Yes. FDA refused 3 shipment lines from Harvest Tek de Mexico Spr de Rlde CV between August 25, 2025 and October 16, 2025. The most recent, on October 16, 2025, was grass hay, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Harvest Tek de Mexico Spr de Rlde CV's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 3 lines).
- What is Harvest Tek de Mexico Spr de Rlde CV's FEI number?
- Harvest Tek de Mexico Spr de Rlde CV's FDA Establishment Identifier (FEI) is 3014537000.
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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.