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PT. Ikan Samudera Indonesia

FDA import alert and refusal historyKota Bitung, IndonesiaFEI 3030666230

Recorded by FDA as PT. IKAN SAMUDERA INDONESIA

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Example subjectPT. Ikan Samudera Indonesi added to Import Alert 16-129 (red list)

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As of October 26, 2026, PT. Ikan Samudera Indonesia (Kota Bitung, Indonesia) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for tuna, published by FDA on August 13, 2024, and has 10 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
IA 16-81 · red list
Last import refusal
Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · SALMONELLA
Last warning letter
None found
Last inspection
None on record

Every FDA record for PT. Ikan Samudera Indonesia

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

2025

  1. Import refusal
    Refused, 4 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 802-0101453-9Show 4 lines
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 802-0101453-9Source
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 802-0101453-9Source
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 802-0101453-9Source
    • Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 802-0101453-9Source
    Source

2024

  1. Import refusal
    Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)SALMONELLAEntry 802-0098771-9
    Source
  2. Import alert listing
    Listed on Import Alert 16-81red listTuna
    Source
  3. Import refusal
    Refused, 5 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)LACKS FIRMSALMONELLAEntry 802-0098327-0Show 5 lines
    Source

Refusal charges, in plain English

  • SALMONELLA10 refused lines

    Salmonella

    The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

  • LACKS FIRM5 refused lines

    Manufacturer name and address missing

    The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

Questions about PT. Ikan Samudera Indonesia

Is PT. Ikan Samudera Indonesia on an FDA import alert?
Yes. As of October 26, 2026, PT. Ikan Samudera Indonesia is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for tuna; FDA published the listing on August 13, 2024.
Has FDA refused shipments from PT. Ikan Samudera Indonesia?
Yes. FDA refused 10 shipment lines from PT. Ikan Samudera Indonesia between August 13, 2024 and March 7, 2025. The most recent, on March 7, 2025, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as SALMONELLA (salmonella).
Why did FDA refuse PT. Ikan Samudera Indonesia's shipments?
The most frequent charges are SALMONELLA (salmonella, 10 lines) and LACKS FIRM (manufacturer name and address missing, 5 lines).
What is PT. Ikan Samudera Indonesia's FEI number?
PT. Ikan Samudera Indonesia's FDA Establishment Identifier (FEI) is 3030666230.
Can shipments from PT. Ikan Samudera Indonesia still enter the U.S.?
Shipments of tuna from PT. Ikan Samudera Indonesia 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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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.