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Lambsmead Ltd

⚠️ Moderate Risk

FEI: 3006335951 • London • UNITED KINGDOM

FEI

FEI Number

3006335951

📍

Location

London

🇬🇧
🏢

Address

29 Knights Bridge, , London, , United Kingdom

Moderate Risk

FDA Import Risk Assessment

45.0
LowModerateHighCritical

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

Statistics

7
Total Refusals
2
Unique Violations
9/4/2007
Latest Refusal
7/31/2007
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
70.0×10%
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

24805×

RXPERSONAL

The article appears to be a device which requires a prescription from your doctor.

842×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
9/4/2007
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
2480RXPERSONAL
New Orleans District Office (NOL-DO)
9/4/2007
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
2480RXPERSONAL
New Orleans District Office (NOL-DO)
8/31/2007
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
2480RXPERSONAL
New Orleans District Office (NOL-DO)
8/29/2007
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
2480RXPERSONAL
New Orleans District Office (NOL-DO)
8/29/2007
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
2480RXPERSONAL
New Orleans District Office (NOL-DO)
8/28/2007
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
84RX DEVICE
New Orleans District Office (NOL-DO)
7/31/2007
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
84RX DEVICE
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Lambsmead Ltd's FDA import refusal history?

Lambsmead Ltd (FEI: 3006335951) has 7 FDA import refusal record(s) in our database, spanning from 7/31/2007 to 9/4/2007.

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. Lambsmead Ltd's FEI number is 3006335951.

What types of violations has Lambsmead Ltd received?

Lambsmead Ltd has been cited for 2 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 Lambsmead Ltd come from?

All FDA import refusal data for Lambsmead 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.