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Netuno Alimentos S/a

FDA import alert and refusal historyRecife, BrazilFEI 3004278153

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Example subjectNetuno Alimentos S/ added to Import Alert 16-129 (red list)

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As of October 25, 2026, Netuno Alimentos S/a (Recife, Brazil) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for lobster; spiny lobster, rock lobster; slipper lobster, published by FDA on August 12, 2010, 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 Netuno Alimentos S/a

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

2010

  1. Import alert listing
    Listed on Import Alert 16-81red listLobster; Spiny Lobster, Rock Lobster; Slipper Lobster
    Source

Questions about Netuno Alimentos S/a

Is Netuno Alimentos S/a on an FDA import alert?
Yes. As of October 25, 2026, Netuno Alimentos S/a is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for lobster; spiny lobster, rock lobster; slipper lobster; FDA published the listing on August 12, 2010.
Has FDA refused shipments from Netuno Alimentos S/a?
No FDA import refusals for Netuno Alimentos S/a appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is Netuno Alimentos S/a's FEI number?
Netuno Alimentos S/a's FDA Establishment Identifier (FEI) is 3004278153.
Can shipments from Netuno Alimentos S/a still enter the U.S.?
Shipments of lobster; spiny lobster, rock lobster; slipper lobster from Netuno Alimentos S/a can be detained without physical examination under Import Alert 16-81; 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 subjectNetuno Alimentos S/ 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.