Productos Selectos Lozano S A De C V
FDA import alert and refusal historyNuevo Leon Mexi, MexicoFEI 3000164632
As of October 26, 2026, Productos Selectos Lozano S A De C V (Nuevo Leon Mexi, 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 Productos Selectos Lozano S A De C V
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 Productos Selectos Lozano S A De C V
- Is Productos Selectos Lozano S A De C V on an FDA import alert?
- Yes. As of October 26, 2026, Productos Selectos Lozano S A De C V 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 Productos Selectos Lozano S A De C V?
- No FDA import refusals for Productos Selectos Lozano S A De C V appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Productos Selectos Lozano S A De C V's FEI number?
- Productos Selectos Lozano S A De C V's FDA Establishment Identifier (FEI) is 3000164632.
- Can shipments from Productos Selectos Lozano S A De C V still enter the U.S.?
- Shipments of pepper, hot, n.e.c. (fruit used as vegetable); fruits used as vegetables, n.e.c. from Productos Selectos Lozano S A De C V 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.