Kader Exports Private Limited, Unit 5
FDA import alert and refusal historyMandapam, IndiaFEI 3004338385
As of October 26, 2026, Kader Exports Private Limited, Unit 5 (Mandapam, India) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for frozen crab, published by FDA on October 22, 2009, is also listed on Import Alert 16-35 (green 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 16-81 · red listIA 16-35 · green list
- Last import refusal
- Shrimp and prawns, aquaculture harvested fishery/seafood products · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Kader Exports Private Limited, Unit 5
9 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalRefused, Shrimp and prawns, aquaculture harvested fishery/seafood productsFILTHYVETDRUGRESNITROFURANEntry KM6-1608519-7Source
2022
- Import refusalSource
Refused, 5 lines in one entry: Shrimp and prawns, aquaculture harvested fishery/seafood productsVETDRUGRESEntry KM6-1570681-9Show 5 linesHide lines
- Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsVETDRUGRESEntry KM6-1570681-9Source
- Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsVETDRUGRESEntry KM6-1570681-9Source
- Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsVETDRUGRESEntry KM6-1570681-9Source
- Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsVETDRUGRESEntry KM6-1570681-9Source
- Refused, Shrimp and prawns, aquaculture harvested fishery/seafood productsVETDRUGRESEntry KM6-1570681-9Source
2015
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 16-81red listFrozen crabSource
- Import alert listingListed on Import Alert 16-35green listRaw ShrimpSource
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.
- FILTHY1 refused line
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.
- NITROFURAN1 refused line
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 Kader Exports Private Limited, Unit 5
- Is Kader Exports Private Limited, Unit 5 on an FDA import alert?
- Yes. As of October 26, 2026, Kader Exports Private Limited, Unit 5 is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for frozen crab; FDA published the listing on October 22, 2009.
- Has FDA refused shipments from Kader Exports Private Limited, Unit 5?
- Yes. FDA refused 6 shipment lines from Kader Exports Private Limited, Unit 5 between June 17, 2022 and April 12, 2024. The most recent, on April 12, 2024, was shrimp and prawns, aquaculture harvested fishery/seafood products, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Kader Exports Private Limited, Unit 5's shipments?
- The most frequent charges are VETDRUGRES (animal drug residue, 6 lines) and FILTHY (filthy, putrid or decomposed substance, 1 line).
- When was Kader Exports Private Limited, Unit 5 last inspected by FDA?
- FDA's most recent inspection of Kader Exports Private Limited, Unit 5 with a final classification is dated July 14, 2015 and was classified NAI (No Action Indicated).
- What is Kader Exports Private Limited, Unit 5's FEI number?
- Kader Exports Private Limited, Unit 5's FDA Establishment Identifier (FEI) is 3004338385.
- Can shipments from Kader Exports Private Limited, Unit 5 still enter the U.S.?
- Shipments of frozen crab from Kader Exports Private Limited, Unit 5 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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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.