Francisco Blas Rosas
FDA import alert and refusal historyLos Reyes De Juarez, MexicoFEI 3016192070
Recorded by FDA as FRANCISCO BLAS ROSAS
As of October 26, 2026, Francisco Blas Rosas (Los Reyes De Juarez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for radish, published by FDA on March 5, 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 99-05 · red list
- Last import refusal
- Radish (root & tuber vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Francisco Blas Rosas
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 Francisco Blas Rosas
- Is Francisco Blas Rosas on an FDA import alert?
- Yes. As of October 26, 2026, Francisco Blas Rosas is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for radish; FDA published the listing on March 5, 2024.
- Has FDA refused shipments from Francisco Blas Rosas?
- Yes. FDA refused 2 shipment lines from Francisco Blas Rosas between February 28, 2024 and April 11, 2024. The most recent, on April 11, 2024, was radish (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Francisco Blas Rosas's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Francisco Blas Rosas's FEI number?
- Francisco Blas Rosas's FDA Establishment Identifier (FEI) is 3016192070.
- Can shipments from Francisco Blas Rosas still enter the U.S.?
- Shipments of radish from Francisco Blas Rosas 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.