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Arunalu Products

FDA import alert and refusal historyKatana, Sri LankaFEI 3013359694

Recorded by FDA as ARUNALU PRODUCTS

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Example subjectArunalu Product added to Import Alert 16-129 (red list)

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As of October 26, 2026, Arunalu Products (Katana, Sri Lanka) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for arunalu dry fish headless sprats, published by FDA on June 13, 2016, is also listed on Import Alert 16-74 (red list), and has 4 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Anchovy · LIST INGRE
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Arunalu Products

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

2025

  1. Import refusal
    Refused, AnchovyLIST INGREINCONSPICUMFR INSANUSUAL NAMENUTRIT LBLEntry HA9-0250640-1
    Source

2023

  1. Import refusal
    Refused, AnchovyLIST INGREINCONSPICUMFR INSANUSUAL NAMENUTRIT LBLEntry 8J2-0009041-3
    Source
  2. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2022

  1. Import refusal
    Refused, AnchovyMFR INSANEntry HA9-0220065-8
    Source
  2. Import refusal
    Refused, AnchovyMFR INSANEntry HA9-0210271-4
    Source

2016

  1. Import alert listing
    Listed on Import Alert 99-39red listArunalu Dry Fish Headless Sprats
    Source
  2. Import alert listing
    Listed on Import Alert 16-74red listSprats; Haalmassa; Stolephorus commersonnii; Arunalu Dried Keeramin Fish
    Source

Refusal charges, in plain English

  • MFR INSAN4 refused lines

    Insanitary manufacturing, processing or packing

    The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.

  • INCONSPICU2 refused lines

    Required information not conspicuous

    Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.

  • LIST INGRE2 refused lines

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

  • NUTRIT LBL2 refused lines

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • USUAL NAME2 refused lines

    Common or usual name missing

    The label appeared not to show the common or usual name of the food.

Questions about Arunalu Products

Is Arunalu Products on an FDA import alert?
Yes. As of October 26, 2026, Arunalu Products is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for arunalu dry fish headless sprats; FDA published the listing on June 13, 2016.
Has FDA refused shipments from Arunalu Products?
Yes. FDA refused 4 shipment lines from Arunalu Products between January 19, 2022 and September 8, 2025. The most recent, on September 8, 2025, was anchovy, charged as LIST INGRE (ingredients not listed).
Why did FDA refuse Arunalu Products's shipments?
The most frequent charges are MFR INSAN (insanitary manufacturing, processing or packing, 4 lines) and INCONSPICU (required information not conspicuous, 2 lines).
When was Arunalu Products last inspected by FDA?
FDA's most recent inspection of Arunalu Products with a final classification is dated May 30, 2023 and was classified NAI (No Action Indicated).
What is Arunalu Products's FEI number?
Arunalu Products's FDA Establishment Identifier (FEI) is 3013359694.
Can shipments from Arunalu Products still enter the U.S.?
Shipments of arunalu dry fish headless sprats from Arunalu Products can be detained without physical examination under Import Alert 99-39; 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 subjectArunalu Product 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.