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Pacifico Import Export S A

FDA import alert and refusal historyGuayamas, MexicoFEI 1000109556

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Example subjectPacifico Import Export S added to Import Alert 16-129 (red list)

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As of October 26, 2026, Pacifico Import Export S A (Guayamas, Mexico) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for flounder (arrowtooth, dab, fluke), 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 Pacifico Import Export S A

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 listFlounder (Arrowtooth, Dab, Fluke)
    Source

Questions about Pacifico Import Export S A

Is Pacifico Import Export S A on an FDA import alert?
Yes. As of October 26, 2026, Pacifico Import Export S A is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for flounder (arrowtooth, dab, fluke); FDA published the listing on September 18, 2009.
Has FDA refused shipments from Pacifico Import Export S A?
No FDA import refusals for Pacifico Import Export S A appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Pacifico Import Export S A's FEI number?
Pacifico Import Export S A's FDA Establishment Identifier (FEI) is 1000109556.
Can shipments from Pacifico Import Export S A still enter the U.S.?
Shipments of flounder (arrowtooth, dab, fluke) from Pacifico Import Export S A 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 subjectPacifico Import Export S 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.