Rancho Cardenas S de RL de CV
FDA import alert and refusal historyEnsenada, MexicoFEI 3009885538
As of October 26, 2026, Rancho Cardenas S de RL de CV (Ensenada, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh coriander; cilantro, published by FDA on April 16, 2013, and has no 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
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Rancho Cardenas S de RL de CV
2 records, newest first. Each line links to the FDA page it came from.
2024
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2013
- Import alert listingListed on Import Alert 99-05red listFresh Coriander; CilantroSource
Questions about Rancho Cardenas S de RL de CV
- Is Rancho Cardenas S de RL de CV on an FDA import alert?
- Yes. As of October 26, 2026, Rancho Cardenas S de RL de CV is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh coriander; cilantro; FDA published the listing on April 16, 2013.
- Has FDA refused shipments from Rancho Cardenas S de RL de CV?
- No FDA import refusals for Rancho Cardenas S de RL de CV appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Rancho Cardenas S de RL de CV last inspected by FDA?
- FDA's most recent inspection of Rancho Cardenas S de RL de CV with a final classification is dated January 16, 2024 and was classified NAI (No Action Indicated).
- What is Rancho Cardenas S de RL de CV's FEI number?
- Rancho Cardenas S de RL de CV's FDA Establishment Identifier (FEI) is 3009885538.
- Can shipments from Rancho Cardenas S de RL de CV still enter the U.S.?
- Shipments of fresh coriander; cilantro from Rancho Cardenas S de RL 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.