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Productos Chavez

FDA import alert and refusal historyTijuana, MexicoFEI 3003019294

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Example subjectProductos Chave added to Import Alert 16-129 (red list)

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As of October 25, 2026, Productos Chavez (Tijuana, Mexico) is on the red list of FDA Import Alert 21-12 (Frozen and refrigerated guacamole and avocado products) for avocado, dried or paste; avocado (pit fruit purees), published by FDA on September 16, 2009, 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 Productos Chavez

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

2009

  1. Import alert listing
    Listed on Import Alert 21-12red listAvocado, Dried or Paste; Avocado (Pit Fruit Purees)
    Source

Questions about Productos Chavez

Is Productos Chavez on an FDA import alert?
Yes. As of October 25, 2026, Productos Chavez is on the red list of FDA Import Alert 21-12, “Frozen and refrigerated guacamole and avocado products”, for avocado, dried or paste; avocado (pit fruit purees); FDA published the listing on September 16, 2009.
Has FDA refused shipments from Productos Chavez?
No FDA import refusals for Productos Chavez appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is Productos Chavez's FEI number?
Productos Chavez's FDA Establishment Identifier (FEI) is 3003019294.
Can shipments from Productos Chavez still enter the U.S.?
Shipments of avocado, dried or paste; avocado (pit fruit purees) from Productos Chavez can be detained without physical examination under Import Alert 21-12; 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 subjectProductos Chave 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.