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Lovehoney Mjs Sunflower

⚠️ Moderate Risk

FEI: 3010955014 • Hong Kong • HONG KONG

FEI

FEI Number

3010955014

📍

Location

Hong Kong

🇭🇰

Country

HONG KONG
🏢

Address

Unit 301, , Hong Kong, , Hong Kong

Moderate Risk

FDA Import Risk Assessment

32.6
LowModerateHighCritical

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

Statistics

3
Total Refusals
5
Unique Violations
3/15/2016
Latest Refusal
8/28/2014
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
19.4×10%
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

1182×

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).

162×

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.

32802×

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.

5082×

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.

2231×

FALSE

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.

Refusal History

DateProductViolationsDivision
3/15/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
1/25/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
8/28/2014
78LSTDEVICE, ERECTILE DYSFUNCTION
223FALSE
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Lovehoney Mjs Sunflower's FDA import refusal history?

Lovehoney Mjs Sunflower (FEI: 3010955014) has 3 FDA import refusal record(s) in our database, spanning from 8/28/2014 to 3/15/2016.

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. Lovehoney Mjs Sunflower's FEI number is 3010955014.

What types of violations has Lovehoney Mjs Sunflower received?

Lovehoney Mjs Sunflower has been cited for 5 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 Lovehoney Mjs Sunflower come from?

All FDA import refusal data for Lovehoney Mjs Sunflower 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.