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Lh Trading Ltd

⚠️ Moderate Risk

FEI: 3008722819 • Bath • UNITED KINGDOM

FEI

FEI Number

3008722819

📍

Location

Bath

🇬🇧
🏢

Address

100 Locksbrook Roa, , Bath, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

47.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

32
Total Refusals
11
Unique Violations
3/16/2017
Latest Refusal
3/30/2012
Earliest Refusal

Score Breakdown

Violation Severity
59.9×40%
Refusal Volume
56.2×30%
Recency
0.0×20%
Frequency
64.5×10%
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

11818×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

1617×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

328014×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

50811×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

2372×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

111×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

751×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

23001×

DIETARYLBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(B) of the FD&C Act in that the label or labeling fails to identify the product by using the term "dietary supplement", which term may be modified with the name of such an ingredient.

2601×

FALSE

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

38641×

NCONTACT

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(y) of the FD&C Act in that the dietary supplement label fails to bear a domestic address or phone number through which the responsible person (as described in section 761 of the FD&C Act) may receive a report of a serious adverse event with such dietary supplement.

4821×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

Refusal History

DateProductViolationsDivision
3/16/2017
80KMJLUBRICANT, PATIENT
118NOT LISTED
3280FRNMFGREG
New Orleans District Office (NOL-DO)
9/13/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
Division of Southeast Imports (DSEI)
8/29/2016
85NUCLUBRICANT, PATIENT, VAGINAL, LATEX COMPATIBLE
118NOT LISTED
3280FRNMFGREG
Division of Southeast Imports (DSEI)
8/19/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
New Orleans District Office (NOL-DO)
8/16/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
Division of Southeast Imports (DSEI)
8/16/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
Division of Southeast Imports (DSEI)
8/15/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
New Orleans District Office (NOL-DO)
8/10/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
8/9/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
8/9/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
8/5/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
New Orleans District Office (NOL-DO)
8/3/2016
80KMJLUBRICANT, PATIENT
118NOT LISTED
Division of Southeast Imports (DSEI)
7/26/2016
80MMSLUBRICANT, VAGINAL, PATIENT
3280FRNMFGREG
New York District Office (NYK-DO)
5/31/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
5/20/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
New Orleans District Office (NOL-DO)
5/9/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
New Orleans District Office (NOL-DO)
3/16/2016
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
3280FRNMFGREG
New Orleans District Office (NOL-DO)
1/29/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
1/25/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
9/23/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
237NO PMA
New Orleans District Office (NOL-DO)
9/22/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
237NO PMA
3280FRNMFGREG
New Orleans District Office (NOL-DO)
9/22/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
New Orleans District Office (NOL-DO)
9/9/2015
54YCH99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
11UNSAFE COL
2300DIETARYLBL
260FALSE
3864NCONTACT
482NUTRIT LBL
New Orleans District Office (NOL-DO)
4/24/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
Division of Southeast Imports (DSEI)
4/24/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
Division of Southeast Imports (DSEI)
3/16/2015
66VIY99MISCELLANEOUS PATENT MEDICINES, ETC.
118NOT LISTED
75UNAPPROVED
New Orleans District Office (NOL-DO)
3/12/2015
80MMSLUBRICANT, VAGINAL, PATIENT
508NO 510(K)
Division of Southeast Imports (DSEI)
3/3/2015
80MMSLUBRICANT, VAGINAL, PATIENT
508NO 510(K)
Division of Southeast Imports (DSEI)
4/30/2014
85NUCLUBRICANT, PATIENT, VAGINAL, LATEX COMPATIBLE
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)
1/29/2013
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
508NO 510(K)
New Orleans District Office (NOL-DO)
12/14/2012
78LSTDEVICE, ERECTILE DYSFUNCTION
16DIRECTIONS
New Orleans District Office (NOL-DO)
3/30/2012
85HISCONDOM
118NOT LISTED
508NO 510(K)
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Lh Trading Ltd's FDA import refusal history?

Lh Trading Ltd (FEI: 3008722819) has 32 FDA import refusal record(s) in our database, spanning from 3/30/2012 to 3/16/2017.

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. Lh Trading Ltd's FEI number is 3008722819.

What types of violations has Lh Trading Ltd received?

Lh Trading Ltd has been cited for 11 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 Lh Trading Ltd come from?

All FDA import refusal data for Lh Trading 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.