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HARIBO LAKRITS AB

⚠️ Moderate Risk

FEI: 3020606576 • Helsingborg, Skane Lan • SWEDEN

FEI

FEI Number

3020606576

📍

Location

Helsingborg, Skane Lan

🇸🇪

Country

SWEDEN
🏢

Address

La Cours Gata 4, , Helsingborg, Skane Lan, Sweden

Moderate Risk

FDA Import Risk Assessment

41.9
LowModerateHighCritical

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

Statistics

2
Total Refusals
3
Unique Violations
8/27/2025
Latest Refusal
8/22/2025
Earliest Refusal

Score Breakdown

Violation Severity
47.5×40%
Refusal Volume
17.7×30%
Recency
78.0×20%
Frequency
20.0×10%
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

38542×

TPLKUSSLLB

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act because it is a tobacco product in package form that appears to be misbranded under section 903(a)(2)(D) of the FD&C Act in that the label does not provide the statement "sale only allowed in the United States" and the tobacco product is not subject to any exemptions or variations.

35201×

TP FLAVOR

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act in that it is, or purports to be or is represented as, a tobacco product that is subject to a tobacco product standard established under section 907, and violates 907 (a) (1) (A) in that the article appears to contain, as a constituent or additive, an artificial or natural flavor (other than tobacco or menthol) or an herb or spice, that is a characterizing flavor of the tobacco product or tobacco smoke.

38421×

TP NO PMTA

This article is subject to refusal of admission pursuant to section 801(a)(3) of the FD&C Act because it is a tobacco product that FDA has found to be adulterated under section 902(6)(A) of the FD&C Act in that it does not have an FDA marketing order in effect under section 910(c)(1)(A)(i) of the FD&C Act.

Refusal History

DateProductViolationsDivision
8/27/2025
98NCA11NICOTINE POUCH
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
8/22/2025
98NCA11NICOTINE POUCH
3520TP FLAVOR
3842TP NO PMTA
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is HARIBO LAKRITS AB's FDA import refusal history?

HARIBO LAKRITS AB (FEI: 3020606576) has 2 FDA import refusal record(s) in our database, spanning from 8/22/2025 to 8/27/2025.

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. HARIBO LAKRITS AB's FEI number is 3020606576.

What types of violations has HARIBO LAKRITS AB received?

HARIBO LAKRITS AB 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 HARIBO LAKRITS AB come from?

All FDA import refusal data for HARIBO LAKRITS AB 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.