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La Paloma Ma. Gpe. Diaz Perez

FDA import alert and refusal historyGuadalajara, MexicoFEI 3000136224

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Example subjectLa Paloma Ma. Gpe. Diaz Pere added to Import Alert 16-129 (red list)

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As of October 26, 2026, La Paloma Ma. Gpe. Diaz Perez (Guadalajara, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for red guava jam, published by FDA on September 18, 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 La Paloma Ma. Gpe. Diaz Perez

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

2009

  1. Import alert listing
    Listed on Import Alert 45-02red listRed Guava Jam
    Source

Questions about La Paloma Ma. Gpe. Diaz Perez

Is La Paloma Ma. Gpe. Diaz Perez on an FDA import alert?
Yes. As of October 26, 2026, La Paloma Ma. Gpe. Diaz Perez is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for red guava jam; FDA published the listing on September 18, 2009.
Has FDA refused shipments from La Paloma Ma. Gpe. Diaz Perez?
No FDA import refusals for La Paloma Ma. Gpe. Diaz Perez appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is La Paloma Ma. Gpe. Diaz Perez's FEI number?
La Paloma Ma. Gpe. Diaz Perez's FDA Establishment Identifier (FEI) is 3000136224.
Can shipments from La Paloma Ma. Gpe. Diaz Perez still enter the U.S.?
Shipments of red guava jam from La Paloma Ma. Gpe. Diaz Perez can be detained without physical examination under Import Alert 45-02; 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 subjectLa Paloma Ma. Gpe. Diaz Pere 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.