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Lucas Hernan Martin

FDA import alert and refusal historyMendoza, ArgentinaFEI 3014101995

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Example subjectLucas Hernan Marti added to Import Alert 16-129 (red list)

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As of October 26, 2026, Lucas Hernan Martin is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 11, 2018, 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
Garlic bulb (root & tuber vegetable) · PESTICIDE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Lucas Hernan Martin

1 record, newest first. Each line links to the FDA page it came from.

2018

  1. Import refusal
    Refused, Garlic bulb (root & tuber vegetable)PESTICIDEEntry EQF-0011726-9
    Source

Refusal charges, in plain English

  • PESTICIDE1 refused line

    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 Lucas Hernan Martin

Is Lucas Hernan Martin on an FDA import alert?
No listing for Lucas Hernan Martin appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Argentina page.
Has FDA refused shipments from Lucas Hernan Martin?
Yes. FDA refused 1 shipment line from Lucas Hernan Martin on May 11, 2018. The most recent, on May 11, 2018, was garlic bulb (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse Lucas Hernan Martin's shipments?
The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
What is Lucas Hernan Martin's FEI number?
Lucas Hernan Martin's FDA Establishment Identifier (FEI) is 3014101995.

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Example subjectLucas Hernan Marti added to Import Alert 16-129 (red list)

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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.