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Perez Mendoza Mercedes

FDA import alert and refusal historyLos Reyes De Jurez, MexicoFEI 3009783777

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Example subjectPerez Mendoza Mercede added to Import Alert 16-129 (red list)

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As of October 26, 2026, Perez Mendoza Mercedes (Los Reyes De Jurez, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for cactus leaves nopal; fresh green onion, published by FDA on February 27, 2013, 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 Perez Mendoza Mercedes

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

2013

  1. Import alert listing
    Listed on Import Alert 99-05red listCactus Leaves Nopal; Fresh Green Onion
    Source

Questions about Perez Mendoza Mercedes

Is Perez Mendoza Mercedes on an FDA import alert?
Yes. As of October 26, 2026, Perez Mendoza Mercedes is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for cactus leaves nopal; fresh green onion; FDA published the listing on February 27, 2013.
Has FDA refused shipments from Perez Mendoza Mercedes?
No FDA import refusals for Perez Mendoza Mercedes appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Perez Mendoza Mercedes's FEI number?
Perez Mendoza Mercedes's FDA Establishment Identifier (FEI) is 3009783777.
Can shipments from Perez Mendoza Mercedes still enter the U.S.?
Shipments of cactus leaves nopal; fresh green onion from Perez Mendoza Mercedes 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 subjectPerez Mendoza Mercede 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.