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Cuananashi Spr de RL de CV

FDA import alert and refusal historyDistrito Federal, MexicoFEI 3010658818

Recorded by FDA as CUANANASHI SPR DE RL DE CV

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Example subjectCuananashi Spr de RL de C added to Import Alert 16-129 (red list)

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As of October 26, 2026, Cuananashi Spr de RL de CV (Distrito Federal, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for fresh pineapples, published by FDA on April 22, 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 Cuananashi Spr de RL de CV

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 Pineapples
    Source

Questions about Cuananashi Spr de RL de CV

Is Cuananashi Spr de RL de CV on an FDA import alert?
Yes. As of October 26, 2026, Cuananashi Spr de RL de CV is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for fresh pineapples; FDA published the listing on April 22, 2014.
Has FDA refused shipments from Cuananashi Spr de RL de CV?
No FDA import refusals for Cuananashi Spr de RL de CV appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Cuananashi Spr de RL de CV's FEI number?
Cuananashi Spr de RL de CV's FDA Establishment Identifier (FEI) is 3010658818.
Can shipments from Cuananashi Spr de RL de CV still enter the U.S.?
Shipments of fresh pineapples from Cuananashi Spr de RL de CV 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 subjectCuananashi Spr de RL de C 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.