Jesus Ramos Bautista
FDA import alert and refusal historyLos Reyes De Juarez, MexicoFEI 3015461329
As of October 26, 2026, Jesus Ramos Bautista (Los Reyes De Juarez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for celery, published by FDA on October 25, 2022, 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
- Celery (leaf & stem vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Jesus Ramos Bautista
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 Jesus Ramos Bautista
- Is Jesus Ramos Bautista on an FDA import alert?
- Yes. As of October 26, 2026, Jesus Ramos Bautista is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for celery; FDA published the listing on October 25, 2022.
- Has FDA refused shipments from Jesus Ramos Bautista?
- Yes. FDA refused 2 shipment lines from Jesus Ramos Bautista between October 12, 2022 and October 2, 2026. The most recent, on October 2, 2026, was celery (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Jesus Ramos Bautista's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Jesus Ramos Bautista's FEI number?
- Jesus Ramos Bautista's FDA Establishment Identifier (FEI) is 3015461329.
- Can shipments from Jesus Ramos Bautista still enter the U.S.?
- Shipments of celery from Jesus Ramos Bautista 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.