Samuel Reyes Navar
FDA import alert and refusal historyRosario, MexicoFEI 2000043757
Recorded by FDA as SAMUEL REYES NAVAR
As of October 26, 2026, Samuel Reyes Navar (Rosario, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for serrano pepper, hot (fruit used as vegetable), raw, fresh, ambient; serrano 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 Samuel Reyes Navar
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listSerrano Pepper, Hot (Fruit Used as Vegetable), Raw, Fresh, Ambient; Serrano Pepper, Hot (Fruit Used as Vegetable), Raw, Fresh, RefrigeratedSource
Questions about Samuel Reyes Navar
- Is Samuel Reyes Navar on an FDA import alert?
- Yes. As of October 26, 2026, Samuel Reyes Navar is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for serrano pepper, hot (fruit used as vegetable), raw, fresh, ambient; serrano pepper, hot (fruit used as vegetable), raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Samuel Reyes Navar?
- No FDA import refusals for Samuel Reyes Navar appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Samuel Reyes Navar's FEI number?
- Samuel Reyes Navar's FDA Establishment Identifier (FEI) is 2000043757.
- Can shipments from Samuel Reyes Navar still enter the U.S.?
- Shipments of serrano pepper, hot (fruit used as vegetable), raw, fresh, ambient; serrano pepper, hot (fruit used as vegetable), raw, fresh, refrigerated from Samuel Reyes Navar 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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