Campo Monte Sol SA de CV
FDA import alert and refusal historyEl Rosario, MexicoFEI 3014023580
As of October 26, 2026, Campo Monte Sol SA de CV (El Rosario, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for celery, published by FDA on May 16, 2019, 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 Campo Monte Sol SA de CV
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 Campo Monte Sol SA de CV
- Is Campo Monte Sol SA de CV on an FDA import alert?
- Yes. As of October 26, 2026, Campo Monte Sol SA de CV is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for celery; FDA published the listing on May 16, 2019.
- Has FDA refused shipments from Campo Monte Sol SA de CV?
- Yes. FDA refused 2 shipment lines from Campo Monte Sol SA de CV between May 21, 2019 and February 14, 2020. The most recent, on February 14, 2020, was celery (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Campo Monte Sol SA de CV's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Campo Monte Sol SA de CV's FEI number?
- Campo Monte Sol SA de CV's FDA Establishment Identifier (FEI) is 3014023580.
- Can shipments from Campo Monte Sol SA de CV still enter the U.S.?
- Shipments of celery from Campo Monte Sol SA de CV 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.