Cadovimex Seafood Import-Export & Processing
FDA import alert and refusal historyCainuoc District, VietnamFEI 3013301881
As of October 26, 2026, Cadovimex Seafood Import-Export & Processing (Cainuoc District, Vietnam) is on the red list of FDA Import Alert 16-129 (Seafood products: nitrofurans) for freshwater shrimp; macrobrachium rosenbergii, published by FDA on July 14, 2021, is also listed on Import Alert 16-124 (red list), and has 6 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-129 · red listIA 16-124 · red list
- Last import refusal
- Shrimp and prawns, aquaculture harvested fishery/seafood products · VETDRUGRES
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Cadovimex Seafood Import-Export & Processing
9 records, newest first. Each line links to the FDA page it came from.
2022
- Import refusalRefused, Shrimp and prawns, aquaculture harvested fishery/seafood productsVETDRUGRESNITROFURANEntry 082-0426547-7Source
2021
- Import alert listingListed on Import Alert 16-129red listFreshwater Shrimp; Macrobrachium rosenbergiiSource
- Import refusalRefused, Shrimp and prawns, aquaculture harvested fishery/seafood productsVETDRUGRESNITROFURANEntry 082-0418839-8Source
2017
- Import alert listingListed on Import Alert 16-124red listTilapiaSource
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
- Import refusalSource
Refused, 4 lines in one entry: Tilapia, aquaculture harvested fishery/seafood productsVETDRUGRESEntry 417-0317173-0Show 4 linesHide lines
- Refused, Tilapia, aquaculture harvested fishery/seafood productsVETDRUGRESEntry 417-0317173-0Source
- Refused, Tilapia, aquaculture harvested fishery/seafood productsVETDRUGRESEntry 417-0317173-0Source
- Refused, Tilapia, aquaculture harvested fishery/seafood productsVETDRUGRESEntry 417-0317173-0Source
- Refused, Tilapia, aquaculture harvested fishery/seafood productsVETDRUGRESEntry 417-0317173-0Source
Refusal charges, in plain English
- VETDRUGRES6 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.
- NITROFURAN2 refused lines
Nitrofurans
The product appeared to contain nitrofurans, a class of antibiotic drugs, which are treated as an unsafe food additive under section 409 of the FD&C Act.
Questions about Cadovimex Seafood Import-Export & Processing
- Is Cadovimex Seafood Import-Export & Processing on an FDA import alert?
- Yes. As of October 26, 2026, Cadovimex Seafood Import-Export & Processing is on the red list of FDA Import Alert 16-129, “Seafood products: nitrofurans”, for freshwater shrimp; macrobrachium rosenbergii; FDA published the listing on July 14, 2021.
- Has FDA refused shipments from Cadovimex Seafood Import-Export & Processing?
- Yes. FDA refused 6 shipment lines from Cadovimex Seafood Import-Export & Processing between April 13, 2017 and February 1, 2022. The most recent, on February 1, 2022, was shrimp and prawns, aquaculture harvested fishery/seafood products, charged as VETDRUGRES (animal drug residue).
- Why did FDA refuse Cadovimex Seafood Import-Export & Processing's shipments?
- The most frequent charges are VETDRUGRES (animal drug residue, 6 lines) and NITROFURAN (nitrofurans, 2 lines).
- When was Cadovimex Seafood Import-Export & Processing last inspected by FDA?
- FDA's most recent inspection of Cadovimex Seafood Import-Export & Processing with a final classification is dated May 23, 2017 and was classified VAI (Voluntary Action Indicated).
- What is Cadovimex Seafood Import-Export & Processing's FEI number?
- Cadovimex Seafood Import-Export & Processing's FDA Establishment Identifier (FEI) is 3013301881.
- Can shipments from Cadovimex Seafood Import-Export & Processing still enter the U.S.?
- Shipments of freshwater shrimp; macrobrachium rosenbergii from Cadovimex Seafood Import-Export & Processing can be detained without physical examination under Import Alert 16-129; 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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