Rancho Hermanos Perez S.P.R. de R.L.
FDA import alert and refusal historyEjido Punta Colonet, MexicoFEI 3004317985
Recorded by FDA as RANCHO HERMANOS PEREZ S.P.R. DE R.L.
As of October 26, 2026, Rancho Hermanos Perez S.P.R. de R.L. (Ejido Punta Colonet, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for nopales cactus; peppers; pasilla; peppers; jalapeno, published by FDA on September 16, 2009, 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 Hermanos Perez S.P.R. de R.L.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listNopales Cactus; Peppers; pasilla; Peppers; jalapenoSource
Questions about Rancho Hermanos Perez S.P.R. de R.L.
- Is Rancho Hermanos Perez S.P.R. de R.L. on an FDA import alert?
- Yes. As of October 26, 2026, Rancho Hermanos Perez S.P.R. de R.L. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for nopales cactus; peppers; pasilla; peppers; jalapeno; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Rancho Hermanos Perez S.P.R. de R.L.?
- No FDA import refusals for Rancho Hermanos Perez S.P.R. de R.L. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Rancho Hermanos Perez S.P.R. de R.L.'s FEI number?
- Rancho Hermanos Perez S.P.R. de R.L.'s FDA Establishment Identifier (FEI) is 3004317985.
- Can shipments from Rancho Hermanos Perez S.P.R. de R.L. still enter the U.S.?
- Shipments of nopales cactus; peppers; pasilla; peppers; jalapeno from Rancho Hermanos Perez S.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.