Martell, S.A. De C.V.
FDA import alert and refusal historySan Salvador, El SalvadorFEI 3010551137
As of October 26, 2026, Martell, S.A. De C.V. (San Salvador, El Salvador) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for frozen loroco, published by FDA on November 15, 2024, 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 99-08 · red list
- Last import refusal
- Fruits used as vegetables, n.e.c. · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Martell, S.A. De C.V.
3 records, newest first. Each line links to the FDA page it came from.
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 Martell, S.A. De C.V.
- Is Martell, S.A. De C.V. on an FDA import alert?
- Yes. As of October 26, 2026, Martell, S.A. De C.V. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for frozen loroco; FDA published the listing on November 15, 2024.
- Has FDA refused shipments from Martell, S.A. De C.V.?
- Yes. FDA refused 2 shipment lines from Martell, S.A. De C.V. between January 13, 2025 and January 30, 2025. The most recent, on January 30, 2025, was fruits used as vegetables, n.e.c., charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Martell, S.A. De C.V.'s shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Martell, S.A. De C.V.'s FEI number?
- Martell, S.A. De C.V.'s FDA Establishment Identifier (FEI) is 3010551137.
- Can shipments from Martell, S.A. De C.V. still enter the U.S.?
- Shipments of frozen loroco from Martell, S.A. De C.V. can be detained without physical examination under Import Alert 99-08; 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.