Efrain Luna Alducin
FDA import alert and refusal historyTecamachalco, MexicoFEI 3029266371
Recorded by FDA as EFRAIN LUNA ALDUCIN
As of October 25, 2026, Efrain Luna Alducin (Tecamachalco, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for cilantro, published by FDA on November 27, 2023, 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
- Cilantro (leaf & stem vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Efrain Luna Alducin
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 Efrain Luna Alducin
- Is Efrain Luna Alducin on an FDA import alert?
- Yes. As of October 25, 2026, Efrain Luna Alducin is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for cilantro; FDA published the listing on November 27, 2023.
- Has FDA refused shipments from Efrain Luna Alducin?
- Yes. FDA refused 2 shipment lines from Efrain Luna Alducin between October 15, 2023 and November 14, 2023. The most recent, on November 14, 2023, was cilantro (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Efrain Luna Alducin's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Efrain Luna Alducin's FEI number?
- Efrain Luna Alducin's FDA Establishment Identifier (FEI) is 3029266371.
- Can shipments from Efrain Luna Alducin still enter the U.S.?
- Shipments of cilantro from Efrain Luna Alducin 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.