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Cakaudrove Fish

FDA import alert and refusal historySuva, FijiFEI 2000019139

Recorded by FDA as CAKAUDROVE FISH

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Example subjectCakaudrove Fis added to Import Alert 16-129 (red list)

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As of October 26, 2026, Cakaudrove Fish (Suva, Fiji) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for fish, n.e.c., published by FDA on September 18, 2009, is also listed on Import Alert 16-120 (red list), 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 Cakaudrove Fish

2 records, newest first. Each line links to the FDA page it came from.

2009

  1. Import alert listing
    Listed on Import Alert 16-81red listFish, N.E.C.
    Source
  2. Import alert listing
    Listed on Import Alert 16-120red listAll histamine forming species; Mackerel (only Scomberomorus spp eg. Spanish or King)
    Source

Questions about Cakaudrove Fish

Is Cakaudrove Fish on an FDA import alert?
Yes. As of October 26, 2026, Cakaudrove Fish is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for fish, n.e.c.; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Cakaudrove Fish?
No FDA import refusals for Cakaudrove Fish appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Cakaudrove Fish's FEI number?
Cakaudrove Fish's FDA Establishment Identifier (FEI) is 2000019139.
Can shipments from Cakaudrove Fish still enter the U.S.?
Shipments of fish, n.e.c. from Cakaudrove Fish 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 subjectCakaudrove Fis 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.