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LONGHAI GELIN FOODS CO., LTD

⚠️ High Risk

FEI: 3004248242 • Longhai City, Fujian • CHINA

FEI

FEI Number

3004248242

📍

Location

Longhai City, Fujian

🇨🇳

Country

CHINA
🏢

Address

Gangwei Town, , Longhai City, Fujian, China

High Risk

FDA Import Risk Assessment

51.4
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

23
Total Refusals
7
Unique Violations
3/27/2019
Latest Refusal
7/16/2003
Earliest Refusal

Score Breakdown

Violation Severity
86.5×40%
Refusal Volume
51.1×30%
Recency
0.0×20%
Frequency
14.6×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

286011×

VETDRUGRES

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a new animal drug (or conversion product thereof) that is unsafe within the meaning of Section 512. Product contains

29203×

PESTICIDES

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:

93×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

25803×

MFRHACCP

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Act in that it appears to have been prepared, packed or held under insanitary conditions whereby it may have been rendered injurious to health in that it appears to have been processed in violation of 21 CFR 123.6(a) and 123.8(a).

29001×

CHLORAMP

The article appears to contain a food additive, namely chloramphenicol, that is unsafe within the meaning of 21 U.S.C. 348.

2491×

FILTHY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.

2951×

LISTERIA

The article is subject to refusal of admission pursuant to Section 801(a)(3), in that the article appears to contain Listeria monocytogenes, a poisonous and deleterious substance, which may render it injurious to health.

Refusal History

DateProductViolationsDivision
3/27/2019
16XGT06TILAPIA, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2860VETDRUGRES
Division of Northeast Imports (DNEI)
3/27/2019
16XGT06TILAPIA, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2860VETDRUGRES
Division of Northeast Imports (DNEI)
1/18/2019
16XGT06TILAPIA, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2860VETDRUGRES
Division of Northeast Imports (DNEI)
1/18/2019
16XGT06TILAPIA, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2860VETDRUGRES
Division of Northeast Imports (DNEI)
1/18/2019
16XGT06TILAPIA, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2860VETDRUGRES
Division of Northeast Imports (DNEI)
1/18/2019
16XGT06TILAPIA, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2860VETDRUGRES
Division of Northeast Imports (DNEI)
11/13/2018
16XGT06TILAPIA, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
2860VETDRUGRES
Division of Southwest Imports (DSWI)
6/14/2017
16MGD99OTHER AQUATIC ANIMALS, N.E.C.
249FILTHY
Division of Northeast Imports (DNEI)
3/13/2012
16AGD58TILAPIA
2580MFRHACCP
Southwest Import District Office (SWI-DO)
3/7/2012
16AYD58TILAPIA
2580MFRHACCP
Southwest Import District Office (SWI-DO)
2/13/2012
16AYD58TILAPIA
2580MFRHACCP
Southwest Import District Office (SWI-DO)
2/13/2012
16XGT06TILAPIA, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
9SALMONELLA
Los Angeles District Office (LOS-DO)
2/13/2012
16XGT06TILAPIA, AQUACULTURE HARVESTED FISHERY/SEAFOOD PRODUCTS
9SALMONELLA
Los Angeles District Office (LOS-DO)
2/2/2012
16AGT58TILAPIA
9SALMONELLA
New York District Office (NYK-DO)
8/11/2010
16AGT10CATFISH, FRESHWATER (E.G. CHANNEL, BLUE, WHITE, YAQUI, BULLHEAD, FLATHEAD CATFISH)
2860VETDRUGRES
New York District Office (NYK-DO)
8/19/2009
24AGT13SOYBEANS (SEE INDUSTRY 37 FOR 'BEAN CURD')
2920PESTICIDES
New York District Office (NYK-DO)
8/14/2008
24AGT13SOYBEANS (SEE INDUSTRY 37 FOR 'BEAN CURD')
2920PESTICIDES
Los Angeles District Office (LOS-DO)
8/31/2007
24AGT13SOYBEANS (SEE INDUSTRY 37 FOR 'BEAN CURD')
2920PESTICIDES
New York District Office (NYK-DO)
1/25/2005
16JGC01CRAB
2900CHLORAMP
Los Angeles District Office (LOS-DO)
1/25/2005
16JGC01CRAB
2860VETDRUGRES
Los Angeles District Office (LOS-DO)
1/25/2005
16JGC01CRAB
2860VETDRUGRES
Los Angeles District Office (LOS-DO)
2/10/2004
16JEO01CRAB
2860VETDRUGRES
New Orleans District Office (NOL-DO)
7/16/2003
16EGN02CLAMS
295LISTERIA
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is LONGHAI GELIN FOODS CO., LTD's FDA import refusal history?

LONGHAI GELIN FOODS CO., LTD (FEI: 3004248242) has 23 FDA import refusal record(s) in our database, spanning from 7/16/2003 to 3/27/2019.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. LONGHAI GELIN FOODS CO., LTD's FEI number is 3004248242.

What types of violations has LONGHAI GELIN FOODS CO., LTD received?

LONGHAI GELIN FOODS CO., LTD has been cited for 7 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about LONGHAI GELIN FOODS CO., LTD come from?

All FDA import refusal data for LONGHAI GELIN FOODS CO., LTD is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.