Omar e Hernandez
FDA import alert and refusal historyJuarez, MexicoFEI 3013400620
Recorded by FDA as OMAR E HERNANDEZ
As of October 25, 2026, Omar e Hernandez (Juarez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh serrano peppers, published by FDA on December 19, 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
- Serrano pepper, hot (fruit used as vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Omar e Hernandez
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 Omar e Hernandez
- Is Omar e Hernandez on an FDA import alert?
- Yes. As of October 25, 2026, Omar e Hernandez is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh serrano peppers; FDA published the listing on December 19, 2018.
- Has FDA refused shipments from Omar e Hernandez?
- Yes. FDA refused 2 shipment lines from Omar e Hernandez between April 26, 2017 and November 7, 2018. The most recent, on November 7, 2018, was serrano pepper, hot (fruit used as vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Omar e Hernandez's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Omar e Hernandez's FEI number?
- Omar e Hernandez's FDA Establishment Identifier (FEI) is 3013400620.
- Can shipments from Omar e Hernandez still enter the U.S.?
- Shipments of fresh serrano peppers from Omar e Hernandez 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.