Ortitec Sa De Cv
FDA import alert and refusal historyEscuinapa, MexicoFEI 3011354849
As of October 25, 2026, Ortitec Sa De Cv (Escuinapa, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for pepper; jalapeno, published by FDA on February 2, 2016, and has 1 FDA import refusal 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
- Jalapeno pepper, hot (fruit used as vegetable) · POISONOUS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Ortitec Sa De Cv
2 records, newest first. Each line links to the FDA page it came from.
2022
2016
- Import alert listingListed on Import Alert 99-23red listPepper; JalapenoSource
Refusal charges, in plain English
- POISONOUS1 refused line
Poisonous or deleterious substance
The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.
Questions about Ortitec Sa De Cv
- Is Ortitec Sa De Cv on an FDA import alert?
- Yes. As of October 25, 2026, Ortitec Sa De Cv is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for pepper; jalapeno; FDA published the listing on February 2, 2016.
- Has FDA refused shipments from Ortitec Sa De Cv?
- Yes. FDA refused 1 shipment line from Ortitec Sa De Cv on January 3, 2022. The most recent, on January 3, 2022, was jalapeno pepper, hot (fruit used as vegetable), charged as POISONOUS (poisonous or deleterious substance).
- Why did FDA refuse Ortitec Sa De Cv's shipments?
- The most frequent charge is POISONOUS (poisonous or deleterious substance, 1 line).
- What is Ortitec Sa De Cv's FEI number?
- Ortitec Sa De Cv's FDA Establishment Identifier (FEI) is 3011354849.
- Can shipments from Ortitec Sa De Cv still enter the U.S.?
- Shipments of pepper; jalapeno from Ortitec Sa De Cv 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.