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Zhanjiang Evergreen Aquatic Product

FDA import alert and refusal historyZhanjiang, ChinaFEI 3005342238

Recorded by FDA as ZHANJIANG EVERGREEN AQUATIC PRODUCT

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Example subjectZhanjiang Evergreen Aquatic Produc added to Import Alert 16-129 (red list)

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As of October 26, 2026, Zhanjiang Evergreen Aquatic Product (Zhanjiang, China) is on the red list of FDA Import Alert 16-124 (Aquaculture seafood: unapproved drugs) for tilapia, published by FDA on March 7, 2018, is also listed on Import Alert 16-131 (green 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
Tilapia, aquaculture harvested fishery/seafood products · VETDRUGRES
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Zhanjiang Evergreen Aquatic Product

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

2018

  1. Import alert listing
    Listed on Import Alert 16-124red listTilapia
    Source
  2. Import refusal
    Refused, Tilapia, aquaculture harvested fishery/seafood productsVETDRUGRESEntry 788-1658700-6
    Source
  3. Import refusal
    Refused, 2 lines in one entry: Tilapia; Tilapia, aquaculture harvested fishery/seafood productsUNSAFE ADDEntry 002-7130879-3Show 2 lines
    Source
  4. Import refusal
    Refused, Tilapia, aquaculture harvested fishery/seafood productsVETDRUGRESEntry E41-0086588-7
    Source

2017

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

2016

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

2011

  1. Import alert listing
    Listed on Import Alert 16-131green listBreaded Shrimp
    Source

Refusal charges, in plain English

  • UNSAFE ADD2 refused lines

    Food additive unsafe under section 409

    The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

  • VETDRUGRES2 refused lines

    Animal drug residue

    The product appeared to contain a new animal drug, or a conversion product of one, that is unsafe within the meaning of section 512 of the FD&C Act.

Questions about Zhanjiang Evergreen Aquatic Product

Is Zhanjiang Evergreen Aquatic Product on an FDA import alert?
Yes. As of October 26, 2026, Zhanjiang Evergreen Aquatic Product is on the red list of FDA Import Alert 16-124, “Aquaculture seafood: unapproved drugs”, for tilapia; FDA published the listing on March 7, 2018.
Has FDA refused shipments from Zhanjiang Evergreen Aquatic Product?
Yes. FDA refused 4 shipment lines from Zhanjiang Evergreen Aquatic Product between January 26, 2018 and February 28, 2018. The most recent, on February 28, 2018, was tilapia, aquaculture harvested fishery/seafood products, charged as VETDRUGRES (animal drug residue).
Why did FDA refuse Zhanjiang Evergreen Aquatic Product's shipments?
The most frequent charges are UNSAFE ADD (food additive unsafe under section 409, 2 lines) and VETDRUGRES (animal drug residue, 2 lines).
When was Zhanjiang Evergreen Aquatic Product last inspected by FDA?
FDA's most recent inspection of Zhanjiang Evergreen Aquatic Product with a final classification is dated August 31, 2017 and was classified VAI (Voluntary Action Indicated).
What is Zhanjiang Evergreen Aquatic Product's FEI number?
Zhanjiang Evergreen Aquatic Product's FDA Establishment Identifier (FEI) is 3005342238.
Can shipments from Zhanjiang Evergreen Aquatic Product still enter the U.S.?
Shipments of tilapia from Zhanjiang Evergreen Aquatic Product can be detained without physical examination under Import Alert 16-124; 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 subjectZhanjiang Evergreen Aquatic Produc 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.