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Ricardo Javier

FDA import alert and refusal historyToluca,Mexico, MexicoFEI 3001342516

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Example subjectRicardo Javie added to Import Alert 16-129 (red list)

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As of October 26, 2026, Ricardo Javier (Toluca,Mexico, Mexico) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for cilantro (leaf & stem vegetable), raw, fresh, refrigerated, 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 Ricardo Javier

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

2009

  1. Import alert listing
    Listed on Import Alert 99-23red listCilantro (Leaf & Stem Vegetable), Raw, Fresh, Refrigerated
    Source

Questions about Ricardo Javier

Is Ricardo Javier on an FDA import alert?
Yes. As of October 26, 2026, Ricardo Javier is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for cilantro (leaf & stem vegetable), raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Ricardo Javier?
No FDA import refusals for Ricardo Javier appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Ricardo Javier's FEI number?
Ricardo Javier's FDA Establishment Identifier (FEI) is 3001342516.
Can shipments from Ricardo Javier still enter the U.S.?
Shipments of cilantro (leaf & stem vegetable), raw, fresh, refrigerated from Ricardo Javier can be detained without physical examination under Import Alert 99-23; 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 subjectRicardo Javie 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.