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Martha Beatriz Trevino Rivera

FDA import alert and refusal historyCd Reynosa, MexicoFEI 3008818229

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Example subjectMartha Beatriz Trevino River added to Import Alert 16-129 (red list)

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As of October 26, 2026, Martha Beatriz Trevino Rivera (Cd Reynosa, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for jalapeno peppers, published by FDA on June 16, 2011, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Martha Beatriz Trevino Rivera

1 record, newest first. Each line links to the FDA page it came from.

2011

  1. Import alert listing
    Listed on Import Alert 99-05red listJalapeno Peppers
    Source

Questions about Martha Beatriz Trevino Rivera

Is Martha Beatriz Trevino Rivera on an FDA import alert?
Yes. As of October 26, 2026, Martha Beatriz Trevino Rivera is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for jalapeno peppers; FDA published the listing on June 16, 2011.
Has FDA refused shipments from Martha Beatriz Trevino Rivera?
No FDA import refusals for Martha Beatriz Trevino Rivera appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Martha Beatriz Trevino Rivera's FEI number?
Martha Beatriz Trevino Rivera's FDA Establishment Identifier (FEI) is 3008818229.
Can shipments from Martha Beatriz Trevino Rivera still enter the U.S.?
Shipments of jalapeno peppers from Martha Beatriz Trevino Rivera 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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Example subjectMartha Beatriz Trevino River added to Import Alert 16-129 (red list)

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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.