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Magdaleno Martinez Carrillo

FDA import alert and refusal historySan Francisco, MexicoFEI 3007602483

Recorded by FDA as MAGDALENO MARTINEZ CARRILLO

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Example subjectMagdaleno Martinez Carrill added to Import Alert 16-129 (red list)

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As of October 26, 2026, Magdaleno Martinez Carrillo (San Francisco, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for papayas, published by FDA on February 25, 2010, 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 Magdaleno Martinez Carrillo

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

2010

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

Questions about Magdaleno Martinez Carrillo

Is Magdaleno Martinez Carrillo on an FDA import alert?
Yes. As of October 26, 2026, Magdaleno Martinez Carrillo is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for papayas; FDA published the listing on February 25, 2010.
Has FDA refused shipments from Magdaleno Martinez Carrillo?
No FDA import refusals for Magdaleno Martinez Carrillo appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Magdaleno Martinez Carrillo's FEI number?
Magdaleno Martinez Carrillo's FDA Establishment Identifier (FEI) is 3007602483.
Can shipments from Magdaleno Martinez Carrillo still enter the U.S.?
Shipments of papayas from Magdaleno Martinez Carrillo 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 subjectMagdaleno Martinez Carrill 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.