PT Bandar Nelayan
FDA import alert and refusal historyDenpasar, IndonesiaFEI 3008861400
As of October 26, 2026, PT Bandar Nelayan (Denpasar, Indonesia) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for tuna, published by FDA on April 1, 2026, and has 22 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-105 · red list
- Last import refusal
- Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · HISTAMINE
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for PT Bandar Nelayan
25 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 224-5109727-7Source
- Import alert listingListed on Import Alert 16-105red listTunaSource
- Import refusalSource
2025
2024
2022
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 224-4873406-5Source
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 224-4873407-3Source
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 224-4873404-0Source
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 224-4872893-5Source
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 224-4872663-2Source
- Import refusalSource
Refused, 2 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYUSUAL NAMEEntry 224-4872658-2Show 2 linesHide lines
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYUSUAL NAMEEntry 224-4872658-2Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYUSUAL NAMEEntry 224-4872658-2Source
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 224-4872656-6Source
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 224-4869979-7Source
- Import refusalSource
Refused, 4 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry BDD-0687916-3Show 4 linesHide lines
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry BDD-0687916-3Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry BDD-0687916-3Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry BDD-0687916-3Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry BDD-0687916-3Source
- Import refusalSource
Refused, 4 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 224-4865356-2Show 4 linesHide lines
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 224-4865356-2Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 224-4865356-2Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 224-4865356-2Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 224-4865356-2Source
Show 3 earlier records (2016–2021)Hide earlier records
2021
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYLACKS FIRMLACKS N/CNUTRIT LBLEntry 417-0357259-8Source
2020
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Refusal charges, in plain English
- FILTHY21 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
- HISTAMINE2 refused lines
Histamine
The product appeared to contain histamine in a quantity that ordinarily makes it injurious to health.
- USUAL NAME2 refused lines
Common or usual name missing
The label appeared not to show the common or usual name of the food.
- LACKS FIRM1 refused line
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.
- LACKS N/C1 refused line
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- NUTRIT LBL1 refused line
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
Questions about PT Bandar Nelayan
- Is PT Bandar Nelayan on an FDA import alert?
- Yes. As of October 26, 2026, PT Bandar Nelayan is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for tuna; FDA published the listing on April 1, 2026.
- Has FDA refused shipments from PT Bandar Nelayan?
- Yes. FDA refused 22 shipment lines from PT Bandar Nelayan between September 28, 2021 and July 16, 2026. The most recent, on July 16, 2026, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as HISTAMINE (histamine).
- Why did FDA refuse PT Bandar Nelayan's shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 21 lines) and HISTAMINE (histamine, 2 lines).
- When was PT Bandar Nelayan last inspected by FDA?
- FDA's most recent inspection of PT Bandar Nelayan with a final classification is dated March 6, 2020 and was classified VAI (Voluntary Action Indicated).
- What is PT Bandar Nelayan's FEI number?
- PT Bandar Nelayan's FDA Establishment Identifier (FEI) is 3008861400.
- Can shipments from PT Bandar Nelayan still enter the U.S.?
- Shipments of tuna from PT Bandar Nelayan can be detained without physical examination under Import Alert 16-105; 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.