Bubs Godis
⚠️ High Risk
FEI: 3009943698 • Jonkoping, Jonkopings Lan • SWEDEN
FEI Number
3009943698
Location
Jonkoping, Jonkopings Lan
Country
SWEDENAddress
Beta Vaegen 4, , Jonkoping, Jonkopings Lan, Sweden
High Risk
FDA Import Risk Assessment
This firm has a significant history of FDA import refusals with notable violations.
Statistics
Score Breakdown
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
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)).
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).
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.
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.
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.
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 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. | Division of West Coast Imports (DWCI) | |
| 10/8/2025 | 33EGT05CANDY BAR OR PIECES (NOT CARAMEL OR FONDANT), HARD, WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | Division of Southeast Imports (DSEI) | |
| 8/22/2025 | 98NCA11NICOTINE POUCH | 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.