Juventino Lozano Cavasos
FDA import alert and refusal historySan Nicolas de los garza, MexicoFEI 3002683837
As of October 26, 2026, Juventino Lozano Cavasos (San Nicolas de los garza, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for pepper, hot, n.e.c. (fruit used as vegetable); fruits used as vegetables, n.e.c., 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 99-23 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Juventino Lozano Cavasos
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-23red listPepper, Hot, N.E.C. (Fruit Used as Vegetable); Fruits Used as Vegetables, N.E.C.Source
Questions about Juventino Lozano Cavasos
- Is Juventino Lozano Cavasos on an FDA import alert?
- Yes. As of October 26, 2026, Juventino Lozano Cavasos is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for pepper, hot, n.e.c. (fruit used as vegetable); fruits used as vegetables, n.e.c.; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Juventino Lozano Cavasos?
- No FDA import refusals for Juventino Lozano Cavasos appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Juventino Lozano Cavasos's FEI number?
- Juventino Lozano Cavasos's FDA Establishment Identifier (FEI) is 3002683837.
- Can shipments from Juventino Lozano Cavasos still enter the U.S.?
- Shipments of pepper, hot, n.e.c. (fruit used as vegetable); fruits used as vegetables, n.e.c. from Juventino Lozano Cavasos can be detained without physical examination under Import Alert 99-23; 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.