Octavio Perez Elisa
FDA import alert and refusal historyGuadalajara, MexicoFEI 3011306169
Recorded by FDA as OCTAVIO PEREZ ELISA
As of October 25, 2026, Octavio Perez Elisa (Guadalajara, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh carrots, published by FDA on December 20, 2018, 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 Octavio Perez Elisa
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 Octavio Perez Elisa
- Is Octavio Perez Elisa on an FDA import alert?
- Yes. As of October 25, 2026, Octavio Perez Elisa is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh carrots; FDA published the listing on December 20, 2018.
- Has FDA refused shipments from Octavio Perez Elisa?
- Yes. FDA refused 2 shipment lines from Octavio Perez Elisa between December 4, 2018 and April 21, 2020. The most recent, on April 21, 2020, was carrot (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Octavio Perez Elisa's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Octavio Perez Elisa's FEI number?
- Octavio Perez Elisa's FDA Establishment Identifier (FEI) is 3011306169.
- Can shipments from Octavio Perez Elisa still enter the U.S.?
- Shipments of fresh carrots from Octavio Perez Elisa 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.