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Alcon Laboratories

⚠️ Moderate Risk

FEI: 3005960666 • Cork, Co. CORK • IRELAND

FEI

FEI Number

3005960666

📍

Location

Cork, Co. CORK

🇮🇪

Country

IRELAND
🏢

Address

Airport East Business & Technology Park, , Cork, Co. CORK, Ireland

Moderate Risk

FDA Import Risk Assessment

27.0
LowModerateHighCritical

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

Statistics

1
Total Refusals
3
Unique Violations
5/17/2016
Latest Refusal
5/17/2016
Earliest Refusal

Score Breakdown

Violation Severity
56.7×40%
Refusal Volume
11.2×30%
Recency
0.0×20%
Frequency
10.0×10%
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

1181×

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).

24801×

RXPERSONAL

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

32801×

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.

Refusal History

DateProductViolationsDivision
5/17/2016
86MFKLENS, MULTIFOCAL INTRAOCULAR
118NOT LISTED
2480RXPERSONAL
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Alcon Laboratories's FDA import refusal history?

Alcon Laboratories (FEI: 3005960666) has 1 FDA import refusal record(s) in our database, spanning from 5/17/2016 to 5/17/2016.

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. Alcon Laboratories's FEI number is 3005960666.

What types of violations has Alcon Laboratories received?

Alcon Laboratories has been cited for 3 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 Alcon Laboratories come from?

All FDA import refusal data for Alcon Laboratories 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.