Rancho Cardenas Ibarra, S. de P.R. de R.L.
FDA import alert and refusal historyEnsenada, MexicoFEI 3007093511
Recorded by FDA as RANCHO CARDENAS IBARRA, S. DE P.R. DE R.L.
As of October 27, 2026, Rancho Cardenas Ibarra, S. de P.R. de R.L. (Ensenada, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for cactus leaves; fresh chard; purslane, published by FDA on August 20, 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
- None on record
Every FDA record for Rancho Cardenas Ibarra, S. de P.R. de R.L.
1 record, newest first. Each line links to the FDA page it came from.
2013
- Import alert listingListed on Import Alert 99-05red listCactus Leaves; Fresh Chard; PurslaneSource
Questions about Rancho Cardenas Ibarra, S. de P.R. de R.L.
- Is Rancho Cardenas Ibarra, S. de P.R. de R.L. on an FDA import alert?
- Yes. As of October 27, 2026, Rancho Cardenas Ibarra, S. de P.R. de R.L. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for cactus leaves; fresh chard; purslane; FDA published the listing on August 20, 2013.
- Has FDA refused shipments from Rancho Cardenas Ibarra, S. de P.R. de R.L.?
- No FDA import refusals for Rancho Cardenas Ibarra, S. de P.R. de R.L. appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Rancho Cardenas Ibarra, S. de P.R. de R.L.'s FEI number?
- Rancho Cardenas Ibarra, S. de P.R. de R.L.'s FDA Establishment Identifier (FEI) is 3007093511.
- Can shipments from Rancho Cardenas Ibarra, S. de P.R. de R.L. still enter the U.S.?
- Shipments of cactus leaves; fresh chard; purslane from Rancho Cardenas Ibarra, S. de P.R. de R.L. 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.