La Corsaria S.A.S
FDA import alert and refusal historyBogota, ColombiaFEI 3017880616
Recorded by FDA as LA CORSARIA S.A.S
As of October 26, 2026, La Corsaria S.A.S (Bogota, Colombia) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for thyme, published by FDA on December 12, 2022, and has 4 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-05 · red list
- Last import refusal
- Thyme, whole (spice) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for La Corsaria S.A.S
5 records, newest first. Each line links to the FDA page it came from.
2023
2022
Refusal charges, in plain English
- PESTICIDE4 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 La Corsaria S.A.S
- Is La Corsaria S.A.S on an FDA import alert?
- Yes. As of October 26, 2026, La Corsaria S.A.S is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for thyme; FDA published the listing on December 12, 2022.
- Has FDA refused shipments from La Corsaria S.A.S?
- Yes. FDA refused 4 shipment lines from La Corsaria S.A.S between November 30, 2022 and February 23, 2023. The most recent, on February 23, 2023, was thyme, whole (spice), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse La Corsaria S.A.S's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 4 lines).
- What is La Corsaria S.A.S's FEI number?
- La Corsaria S.A.S's FDA Establishment Identifier (FEI) is 3017880616.
- Can shipments from La Corsaria S.A.S still enter the U.S.?
- Shipments of thyme from La Corsaria S.A.S can be detained without physical examination under Import Alert 99-05; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.