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Laboratorio Ecar SA

FDA import alert and refusal historyAntioguia, ColombiaFEI 3043301450

Recorded by FDA as LABORATORIO ECAR SA

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Example subjectLaboratorio Ecar S added to Import Alert 16-129 (red list)

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As of October 26, 2026, Laboratorio Ecar SA is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 10, 2026, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Vitamin b12 (cyanocobalamin) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Laboratorio Ecar SA

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

2026

  1. Import refusal
    Refused, Vitamin b12 (cyanocobalamin)UNAPPROVEDEntry AEK-0766814-7
    Source

Refusal charges, in plain English

  • UNAPPROVED1 refused line

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Laboratorio Ecar SA

Is Laboratorio Ecar SA on an FDA import alert?
No listing for Laboratorio Ecar SA appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Colombia page.
Has FDA refused shipments from Laboratorio Ecar SA?
Yes. FDA refused 1 shipment line from Laboratorio Ecar SA on July 10, 2026. The most recent, on July 10, 2026, was vitamin b12 (cyanocobalamin), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Laboratorio Ecar SA's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Laboratorio Ecar SA's FEI number?
Laboratorio Ecar SA's FDA Establishment Identifier (FEI) is 3043301450.

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Example subjectLaboratorio Ecar S 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.