Luis Rojas
FDA import alert and refusal historyValle Vizcaino, MexicoFEI 3007094400
Recorded by FDA as LUIS ROJAS
As of October 25, 2026, Luis Rojas (VALLE VIZCAINO, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for jalapeno pepper, hot (fruit used as vegetable), raw, fresh, ambient; jalapeno pepper, hot (fruit used as vegetable), raw, fresh, refrigerated, 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 Luis Rojas
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listJalapeno Pepper, Hot (Fruit Used as Vegetable), Raw, Fresh, Ambient; Jalapeno Pepper, Hot (Fruit Used as Vegetable), Raw, Fresh, RefrigeratedSource
Questions about Luis Rojas
- Is Luis Rojas on an FDA import alert?
- Yes. As of October 25, 2026, Luis Rojas is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for jalapeno pepper, hot (fruit used as vegetable), raw, fresh, ambient; jalapeno pepper, hot (fruit used as vegetable), raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Luis Rojas?
- No FDA import refusals for Luis Rojas appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Luis Rojas's FEI number?
- Luis Rojas's FDA Establishment Identifier (FEI) is 3007094400.
- Can shipments from Luis Rojas still enter the U.S.?
- Shipments of jalapeno pepper, hot (fruit used as vegetable), raw, fresh, ambient; jalapeno pepper, hot (fruit used as vegetable), raw, fresh, refrigerated from Luis Rojas 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.