Rancho la Loma
FDA import alert and refusal historySan Francisco Del Rin, MexicoFEI 3013217161
Recorded by FDA as RANCHO LA LOMA
As of October 25, 2026, Rancho la Loma (San Francisco Del Rin, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh celery, published by FDA on December 26, 2017, 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 Rancho la Loma
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 Rancho la Loma
- Is Rancho la Loma on an FDA import alert?
- Yes. As of October 25, 2026, Rancho la Loma is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh celery; FDA published the listing on December 26, 2017.
- Has FDA refused shipments from Rancho la Loma?
- Yes. FDA refused 2 shipment lines from Rancho la Loma between December 19, 2017 and December 20, 2017. The most recent, on December 20, 2017, was celery (leaf & stem vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Rancho la Loma's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Rancho la Loma's FEI number?
- Rancho la Loma's FDA Establishment Identifier (FEI) is 3013217161.
- Can shipments from Rancho la Loma still enter the U.S.?
- Shipments of fresh celery from Rancho la Loma 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.