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Emergency

⚠️ Moderate Risk

FEI: 3003477046 • Saint-Laurent, QC • CANADA

FEI

FEI Number

3003477046

📍

Location

Saint-Laurent, QC

🇨🇦

Country

CANADA
🏢

Address

700 Lebeau Blvd, , Saint-Laurent, QC, Canada

Moderate Risk

FDA Import Risk Assessment

31.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
6/9/2011
Latest Refusal
12/16/2010
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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).

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

4771×

HOLES

The quality of the article falls below that which it purports or is represented to possess, in that the devices contain defects/holes.

4791×

DV QUALITY

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be adulterated since its strength differs from, or its purity or quality falls below, that which it purports or is represented to possess.

Refusal History

DateProductViolationsDivision
6/9/2011
79OHOFIRST AID KIT WITHOUT DRUG
118NOT LISTED
341REGISTERED
New York District Office (NYK-DO)
12/20/2010
79OHOFIRST AID KIT WITHOUT DRUG
477HOLES
New York District Office (NYK-DO)
12/16/2010
79OHOFIRST AID KIT WITHOUT DRUG
479DV QUALITY
New York District Office (NYK-DO)

Frequently Asked Questions

What is Emergency's FDA import refusal history?

Emergency (FEI: 3003477046) has 3 FDA import refusal record(s) in our database, spanning from 12/16/2010 to 6/9/2011.

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. Emergency's FEI number is 3003477046.

What types of violations has Emergency received?

Emergency has been cited for 4 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 Emergency come from?

All FDA import refusal data for Emergency 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.