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Unilever Canada

⚠️ Moderate Risk

FEI: 3004802979 • Toronto • CANADA

FEI

FEI Number

3004802979

📍

Location

Toronto

🇨🇦

Country

CANADA
🏢

Address

160 Bloor Street East, , Toronto, , Canada

Moderate Risk

FDA Import Risk Assessment

33.4
LowModerateHighCritical

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

Statistics

5
Total Refusals
6
Unique Violations
11/16/2023
Latest Refusal
3/29/2007
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
28.8×30%
Recency
42.4×20%
Frequency
3.0×10%
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

3212×

LACKS N/C

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

4712×

CSTIC LBLG

The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.

4822×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

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).

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.

3351×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

Refusal History

DateProductViolationsDivision
11/16/2023
27AGT02MAYONNAISE
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
10/30/2023
27AYT02MAYONNAISE
321LACKS N/C
482NUTRIT LBL
Division of Northern Border Imports (DNBI)
6/9/2023
61HAY05ZINC PYRITHIONE (ANTI-BACTERIAL)
118NOT LISTED
3280FRNMFGREG
335LACKS N/C
Division of Northern Border Imports (DNBI)
3/29/2007
53ED01HAIR CONDITIONERS (HAIR PREPARATIONS, NON-COLORING)
471CSTIC LBLG
New York District Office (NYK-DO)
3/29/2007
53ED06SHAMPOOS (HAIR PREPARATIONS, NON-COLORING)
471CSTIC LBLG
New York District Office (NYK-DO)

Frequently Asked Questions

What is Unilever Canada's FDA import refusal history?

Unilever Canada (FEI: 3004802979) has 5 FDA import refusal record(s) in our database, spanning from 3/29/2007 to 11/16/2023.

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. Unilever Canada's FEI number is 3004802979.

What types of violations has Unilever Canada received?

Unilever Canada has been cited for 6 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 Unilever Canada come from?

All FDA import refusal data for Unilever Canada 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.