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Santa Cecilia Zamora Reyes

FDA import alert and refusal historyMazatln, MexicoFEI 3010594908

Recorded by FDA as SANTA CECILIA ZAMORA REYES

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Example subjectSanta Cecilia Zamora Reye added to Import Alert 16-129 (red list)

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As of October 26, 2026, Santa Cecilia Zamora Reyes (Mazatln, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh anaheim peppers, published by FDA on June 6, 2014, 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 Santa Cecilia Zamora Reyes

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

2014

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

Questions about Santa Cecilia Zamora Reyes

Is Santa Cecilia Zamora Reyes on an FDA import alert?
Yes. As of October 26, 2026, Santa Cecilia Zamora Reyes is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh anaheim peppers; FDA published the listing on June 6, 2014.
Has FDA refused shipments from Santa Cecilia Zamora Reyes?
No FDA import refusals for Santa Cecilia Zamora Reyes appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Santa Cecilia Zamora Reyes's FEI number?
Santa Cecilia Zamora Reyes's FDA Establishment Identifier (FEI) is 3010594908.
Can shipments from Santa Cecilia Zamora Reyes still enter the U.S.?
Shipments of fresh anaheim peppers from Santa Cecilia Zamora Reyes 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 subjectSanta Cecilia Zamora 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.