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Comercializadora Mexicana De Legumbres S.A. de C.V.

FDA import alert and refusal historyAsientos, MexicoFEI 3001691817

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Example subjectComercializadora Mexicana De Legumbres S.A. de C.V added to Import Alert 16-129 (red list)

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As of October 27, 2026, Comercializadora Mexicana De Legumbres S.A. de C.V. (Asientos, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for cactus pads, published by FDA on June 14, 2018, 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 Comercializadora Mexicana De Legumbres S.A. de C.V.

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

2018

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

Questions about Comercializadora Mexicana De Legumbres S.A. de C.V.

Is Comercializadora Mexicana De Legumbres S.A. de C.V. on an FDA import alert?
Yes. As of October 27, 2026, Comercializadora Mexicana De Legumbres S.A. de C.V. is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for cactus pads; FDA published the listing on June 14, 2018.
Has FDA refused shipments from Comercializadora Mexicana De Legumbres S.A. de C.V.?
No FDA import refusals for Comercializadora Mexicana De Legumbres S.A. de C.V. appear in FDA's refusal data since October 2016, as of October 27, 2026.
What is Comercializadora Mexicana De Legumbres S.A. de C.V.'s FEI number?
Comercializadora Mexicana De Legumbres S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3001691817.
Can shipments from Comercializadora Mexicana De Legumbres S.A. de C.V. still enter the U.S.?
Shipments of cactus pads from Comercializadora Mexicana De Legumbres S.A. de C.V. 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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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.