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Dr.Numb

⚠️ Moderate Risk

FEI: 3012019423 • Vancouver, British Columbia • CANADA

FEI

FEI Number

3012019423

📍

Location

Vancouver, British Columbia

🇨🇦

Country

CANADA
🏢

Address

4196 Staulo Cres, , Vancouver, British Columbia, Canada

Moderate Risk

FDA Import Risk Assessment

47.1
LowModerateHighCritical

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

Statistics

10
Total Refusals
5
Unique Violations
7/6/2016
Latest Refusal
1/22/2016
Earliest Refusal

Score Breakdown

Violation Severity
63.8×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

758×

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).

1185×

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).

32805×

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.

3362×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

Refusal History

DateProductViolationsDivision
7/6/2016
60QKO67LIDOCAINE (ANESTHETIC)
75UNAPPROVED
Cincinnati District Office (CIN-DO)
7/1/2016
60QAO67LIDOCAINE (ANESTHETIC)
75UNAPPROVED
Cincinnati District Office (CIN-DO)
6/17/2016
60QBY67LIDOCAINE (ANESTHETIC)
75UNAPPROVED
Cincinnati District Office (CIN-DO)
4/4/2016
60QBO07LIDOCAINE
118NOT LISTED
3280FRNMFGREG
473LABELING
75UNAPPROVED
Cincinnati District Office (CIN-DO)
3/31/2016
60QAY07LIDOCAINE
75UNAPPROVED
Cincinnati District Office (CIN-DO)
3/29/2016
60QAY07LIDOCAINE
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Cincinnati District Office (CIN-DO)
3/29/2016
60QAY07LIDOCAINE
75UNAPPROVED
Cincinnati District Office (CIN-DO)
3/16/2016
60QAJ67LIDOCAINE (ANESTHETIC)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
Seattle District Office (SEA-DO)
2/17/2016
60QAJ67LIDOCAINE (ANESTHETIC)
118NOT LISTED
3280FRNMFGREG
336INCONSPICU
Seattle District Office (SEA-DO)
1/22/2016
60QIY67LIDOCAINE (ANESTHETIC)
118NOT LISTED
3280FRNMFGREG
75UNAPPROVED
Cincinnati District Office (CIN-DO)

Frequently Asked Questions

What is Dr.Numb's FDA import refusal history?

Dr.Numb (FEI: 3012019423) has 10 FDA import refusal record(s) in our database, spanning from 1/22/2016 to 7/6/2016.

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. Dr.Numb's FEI number is 3012019423.

What types of violations has Dr.Numb received?

Dr.Numb 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 Dr.Numb come from?

All FDA import refusal data for Dr.Numb 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.