Aldo Rosas Flores
FDA import alert and refusal historyTepeaca, MexicoFEI 3012351095
Recorded by FDA as ALDO ROSAS FLORES
As of October 26, 2026, Aldo Rosas Flores (Tepeaca, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for coriander (cilantro), published by FDA on February 1, 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
- Cilantro (leaf & stem vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Aldo Rosas Flores
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 Aldo Rosas Flores
- Is Aldo Rosas Flores on an FDA import alert?
- Yes. As of October 26, 2026, Aldo Rosas Flores is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for coriander (cilantro); FDA published the listing on February 1, 2018.
- Has FDA refused shipments from Aldo Rosas Flores?
- Yes. FDA refused 2 shipment lines from Aldo Rosas Flores between February 5, 2018 and February 13, 2018. The most recent, on February 13, 2018, was cilantro (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Aldo Rosas Flores's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Aldo Rosas Flores's FEI number?
- Aldo Rosas Flores's FDA Establishment Identifier (FEI) is 3012351095.
- Can shipments from Aldo Rosas Flores still enter the U.S.?
- Shipments of coriander (cilantro) from Aldo Rosas Flores 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.