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Castlerock Fisheries Pvt Ltd.

FDA import alert and refusal historyTaloja, IndiaFEI 13209

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Example subjectCastlerock Fisheries Pvt Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Castlerock Fisheries Pvt Ltd. (Taloja, India) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for bream, published by FDA on September 18, 2009, is also listed on Import Alert 16-23 (green list) and Import Alert 16-35 (green list), and has 3 FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
Shrimp and prawns, aquaculture harvested fishery/seafood products · FILTHY
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Castlerock Fisheries Pvt Ltd.

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

2021

  1. Import refusal
    Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsFILTHYSALMONELLAEntry AQZ-0488085-5
    Source

2020

  1. Import refusal
    Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsFILTHYEntry AQZ-0488049-1
    Source
  2. Import refusal
    Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsFILTHYEntry AQZ-0493608-7
    Source

2017

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
    Source

2014

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2010

  1. Import alert listing
    Listed on Import Alert 16-23green listLobster; Spiny Lobster, Rock Lobster
    Source

2009

  1. Import alert listing
    Listed on Import Alert 16-81red listBream
    Source
  2. Import alert listing
    Listed on Import Alert 16-35green listRaw Shrimp; Cooked Shrimp
    Source

Refusal charges, in plain English

  • FILTHY3 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.

  • SALMONELLA1 refused line

    Salmonella

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

Questions about Castlerock Fisheries Pvt Ltd.

Is Castlerock Fisheries Pvt Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Castlerock Fisheries Pvt Ltd. is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for bream; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Castlerock Fisheries Pvt Ltd.?
Yes. FDA refused 3 shipment lines from Castlerock Fisheries Pvt Ltd. between November 10, 2020 and April 1, 2021. The most recent, on April 1, 2021, was shrimp and prawns, aquaculture harvested fishery/seafood products, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Castlerock Fisheries Pvt Ltd.'s shipments?
The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 3 lines) and SALMONELLA (salmonella, 1 line).
When was Castlerock Fisheries Pvt Ltd. last inspected by FDA?
FDA's most recent inspection of Castlerock Fisheries Pvt Ltd. with a final classification is dated April 22, 2017 and was classified VAI (Voluntary Action Indicated).
What is Castlerock Fisheries Pvt Ltd.'s FEI number?
Castlerock Fisheries Pvt Ltd.'s FDA Establishment Identifier (FEI) is 13209.
Can shipments from Castlerock Fisheries Pvt Ltd. still enter the U.S.?
Shipments of bream from Castlerock Fisheries Pvt Ltd. 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 subjectCastlerock Fisheries Pvt Ltd 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.