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Bertha Alicia Lopez Ibarra

FDA import alert and refusal historyHuatabampo, MexicoFEI 3011073314

Recorded by FDA as BERTHA ALICIA LOPEZ IBARRA

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Example subjectBertha Alicia Lopez Ibarr added to Import Alert 16-129 (red list)

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As of October 26, 2026, Bertha Alicia Lopez Ibarra (Huatabampo, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for serrano peppers, published by FDA on October 3, 2016, 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 Bertha Alicia Lopez Ibarra

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

2016

  1. Import alert listing
    Listed on Import Alert 99-23red listSerrano Peppers
    Source

Questions about Bertha Alicia Lopez Ibarra

Is Bertha Alicia Lopez Ibarra on an FDA import alert?
Yes. As of October 26, 2026, Bertha Alicia Lopez Ibarra is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for serrano peppers; FDA published the listing on October 3, 2016.
Has FDA refused shipments from Bertha Alicia Lopez Ibarra?
No FDA import refusals for Bertha Alicia Lopez Ibarra appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Bertha Alicia Lopez Ibarra's FEI number?
Bertha Alicia Lopez Ibarra's FDA Establishment Identifier (FEI) is 3011073314.
Can shipments from Bertha Alicia Lopez Ibarra still enter the U.S.?
Shipments of serrano peppers from Bertha Alicia Lopez Ibarra 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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Example subjectBertha Alicia Lopez Ibarr 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.