Coprimex S.A.
FDA import alert and refusal historyCartago, Costa RicaFEI 3012212782
As of October 26, 2026, Coprimex S.A. (Cartago, Costa Rica) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for carrots, published by FDA on March 2, 2026, and has 2 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
- Carrot (root & tuber vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Coprimex S.A.
3 records, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 99-05red listCarrotsSource
- Import refusalSource
Refused, 2 lines in one entry: Carrot (root & tuber vegetable)PESTICIDEEntry DMV-0010574-5Show 2 linesHide lines
Refusal charges, in plain English
- PESTICIDE2 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 Coprimex S.A.
- Is Coprimex S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Coprimex S.A. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for carrots; FDA published the listing on March 2, 2026.
- Has FDA refused shipments from Coprimex S.A.?
- Yes. FDA refused 2 shipment lines from Coprimex S.A. on February 23, 2026. The most recent, on February 23, 2026, was carrot (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Coprimex S.A.'s shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Coprimex S.A.'s FEI number?
- Coprimex S.A.'s FDA Establishment Identifier (FEI) is 3012212782.
- Can shipments from Coprimex S.A. still enter the U.S.?
- Shipments of carrots from Coprimex S.A. 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.