Haelssen & Lyon GmbH
⚠️ Moderate Risk
FEI: 3005130014 • Hamburg, Hamburg • GERMANY
FEI Number
3005130014
Location
Hamburg, Hamburg
Country
GERMANYAddress
Wilhelm-Iwan-Ring 6, , Hamburg, Hamburg, Germany
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
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
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.
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
LACKS FIRM
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)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.
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.
PESTICIDE2
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
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.
INCONSPICU
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)).
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/28/2023 | 31KYT02TEA, GREEN | Division of Southeast Imports (DSEI) | |
| 6/20/2023 | 31MYT01TEA WITH FRUIT (PEELS, CHUNKS, BITS OR PIECES) | Division of Southeast Imports (DSEI) | |
| 6/20/2023 | 31KYT02TEA, GREEN | Division of Southeast Imports (DSEI) | |
| 6/11/2021 | 83QJRREAGENTS, 2019-NOVEL CORONAVIRUS NUCLEIC ACID | 508NO 510(K) | Division of Southeast Imports (DSEI) |
| 6/18/2012 | 20BGH24WOLFBERRY (CHINESE OR SOUTHEAST ASIAN BERRY OF THE CHINESE MATRIMONY VINE, W/SLIGHT LICORICE FLAVOR) | 3721PESTICIDE2 | Division of Northeast Imports (DNEI) |
| 6/18/2012 | 20BGH24WOLFBERRY (CHINESE OR SOUTHEAST ASIAN BERRY OF THE CHINESE MATRIMONY VINE, W/SLIGHT LICORICE FLAVOR) | 3721PESTICIDE2 | Division of Northeast Imports (DNEI) |
| 6/18/2012 | 20BGH24WOLFBERRY (CHINESE OR SOUTHEAST ASIAN BERRY OF THE CHINESE MATRIMONY VINE, W/SLIGHT LICORICE FLAVOR) | 3721PESTICIDE2 | Division of Northeast Imports (DNEI) |
| 12/8/2011 | 20BGH24WOLFBERRY (CHINESE OR SOUTHEAST ASIAN BERRY OF THE CHINESE MATRIMONY VINE, W/SLIGHT LICORICE FLAVOR) | Baltimore District Office (BLT-DO) | |
| 5/25/2011 | 31KAT01TEA, BLACK | 2920PESTICIDES | Southwest Import District Office (SWI-DO) |
| 5/25/2011 | 31KAT99TEA, N.E.C. | 2920PESTICIDES | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Haelssen & Lyon GmbH's FDA import refusal history?
Haelssen & Lyon GmbH (FEI: 3005130014) has 10 FDA import refusal record(s) in our database, spanning from 5/25/2011 to 7/28/2023.
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. Haelssen & Lyon GmbH's FEI number is 3005130014.
What types of violations has Haelssen & Lyon GmbH received?
Haelssen & Lyon GmbH has been cited for 9 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 Haelssen & Lyon GmbH come from?
All FDA import refusal data for Haelssen & Lyon GmbH 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.