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Bubs Godis

⚠️ High Risk

FEI: 3009943698 • Jonkoping, Jonkopings Lan • SWEDEN

FEI

FEI Number

3009943698

📍

Location

Jonkoping, Jonkopings Lan

🇸🇪

Country

SWEDEN
🏢

Address

Beta Vaegen 4, , Jonkoping, Jonkopings Lan, Sweden

High Risk

FDA Import Risk Assessment

58.1
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

9
Total Refusals
8
Unique Violations
10/30/2025
Latest Refusal
1/24/2025
Earliest Refusal

Score Breakdown

Violation Severity
47.1×40%
Refusal Volume
37.0×30%
Recency
95.5×20%
Frequency
90.0×10%
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

3245×

NO ENGLISH

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

112×

UNSAFE COL

The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).

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.

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.

38541×

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.

4731×

LABELING

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

2181×

LIST INGRE

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(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

Refusal History

DateProductViolationsDivision
10/30/2025
33LGT06FLAVORED CANDY, SOFT (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
11UNSAFE COL
Division of Northern Border Imports (DNBI)
10/15/2025
33YYY99CANDY WITHOUT CHOCOLATE N.E.C.
11UNSAFE COL
218LIST INGRE
482NUTRIT LBL
Division of West Coast Imports (DWCI)
10/8/2025
33EGT05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), HARD, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE)
473LABELING
482NUTRIT LBL
Division of Southeast Imports (DSEI)
8/22/2025
98NCA11NICOTINE POUCH
3520TP FLAVOR
3842TP NO PMTA
3854TPLKUSSLLB
Division of Southeast Imports (DSEI)
1/24/2025
33MGT06JELLY FRUIT POPPERS CANDY
324NO ENGLISH
Division of Southeast Imports (DSEI)
1/24/2025
33MGT06JELLY FRUIT POPPERS CANDY
324NO ENGLISH
Division of Southeast Imports (DSEI)
1/24/2025
33MGT06JELLY FRUIT POPPERS CANDY
324NO ENGLISH
Division of Southeast Imports (DSEI)
1/24/2025
33MGT06JELLY FRUIT POPPERS CANDY
324NO ENGLISH
Division of Southeast Imports (DSEI)
1/24/2025
33MGT06JELLY FRUIT POPPERS CANDY
324NO ENGLISH
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Bubs Godis's FDA import refusal history?

Bubs Godis (FEI: 3009943698) has 9 FDA import refusal record(s) in our database, spanning from 1/24/2025 to 10/30/2025.

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. Bubs Godis's FEI number is 3009943698.

What types of violations has Bubs Godis received?

Bubs Godis has been cited for 8 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 Bubs Godis come from?

All FDA import refusal data for Bubs Godis 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.