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Luz Amelia Herrera Reyes

FDA import alert and refusal historyGuadalupe, MexicoFEI 3004380756

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Example subjectLuz Amelia Herrera Reye added to Import Alert 16-129 (red list)

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As of October 26, 2026, Luz Amelia Herrera Reyes (Guadalupe, Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for sardines (brisling, sprats, pilchards, etc.), published by FDA on September 18, 2009, 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 Luz Amelia Herrera Reyes

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

2009

  1. Import alert listing
    Listed on Import Alert 16-81red listSardines (Brisling, Sprats, Pilchards, Etc.)
    Source

Questions about Luz Amelia Herrera Reyes

Is Luz Amelia Herrera Reyes on an FDA import alert?
Yes. As of October 26, 2026, Luz Amelia Herrera Reyes is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for sardines (brisling, sprats, pilchards, etc.); FDA published the listing on September 18, 2009.
Has FDA refused shipments from Luz Amelia Herrera Reyes?
No FDA import refusals for Luz Amelia Herrera Reyes appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Luz Amelia Herrera Reyes's FEI number?
Luz Amelia Herrera Reyes's FDA Establishment Identifier (FEI) is 3004380756.
Can shipments from Luz Amelia Herrera Reyes still enter the U.S.?
Shipments of sardines (brisling, sprats, pilchards, etc.) from Luz Amelia Herrera Reyes can be detained without physical examination under Import Alert 16-81; 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 subjectLuz Amelia Herrera Reye 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.