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Productos Delta CA-Caprodel

FDA import alert and refusal historyDepartamento Antonio Diaz, VenezuelaFEI 9804

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Example subjectProductos Delta CA-Caprode added to Import Alert 16-129 (red list)

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As of October 26, 2026, Productos Delta CA-Caprodel (Departamento Antonio Diaz, Venezuela) is on the red list of FDA Import Alert 99-38 (Low-acid canned/acidified foods: inadequate process control) for hearts of palm, published by FDA on June 3, 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 Productos Delta CA-Caprodel

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

2014

  1. Import alert listing
    Listed on Import Alert 99-38red listHearts of palm
    Source

Questions about Productos Delta CA-Caprodel

Is Productos Delta CA-Caprodel on an FDA import alert?
Yes. As of October 26, 2026, Productos Delta CA-Caprodel is on the red list of FDA Import Alert 99-38, “Low-acid canned/acidified foods: inadequate process control”, for hearts of palm; FDA published the listing on June 3, 2014.
Has FDA refused shipments from Productos Delta CA-Caprodel?
No FDA import refusals for Productos Delta CA-Caprodel appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Productos Delta CA-Caprodel's FEI number?
Productos Delta CA-Caprodel's FDA Establishment Identifier (FEI) is 9804.
Can shipments from Productos Delta CA-Caprodel still enter the U.S.?
Shipments of hearts of palm from Productos Delta CA-Caprodel can be detained without physical examination under Import Alert 99-38; 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 Delta CA-Caprode 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.