Haelssen & Lyon GmbH
FDA import alert and refusal historyHamburg, GermanyFEI 3005130014
As of October 26, 2026, Haelssen & Lyon GmbH (Hamburg, Germany) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for gogi berries wolfberries, published by FDA on December 22, 2011, and has 3 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-08 · red list
- Last import refusal
- Tea, green · LIST INGRE
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Haelssen & Lyon GmbH
6 records, newest first. Each line links to the FDA page it came from.
2024
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2023
- Import refusalRefused, Tea, greenLIST INGREINCONSPICULACKS FIRMEntry 799-5967688-3Source
- Import refusalSource
Refused, 2 lines in one entry: Tea with fruit (peels, chunks, bits or pieces); Tea, greenLIST INGRELACKS FIRMLACKS N/CNUTRIT LBLEntry 799-5266583-4Show 2 linesHide lines
- Refused, Tea with fruit (peels, chunks, bits or pieces)LIST INGRELACKS FIRMLACKS N/CNUTRIT LBLEntry 799-5266583-4Source
- Refused, Tea, greenLIST INGRELACKS FIRMLACKS N/CNUTRIT LBLEntry 799-5266583-4Source
2013
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2011
- Import alert listingListed on Import Alert 99-08red listGogi Berries WolfberriesSource
Refusal charges, in plain English
- LACKS FIRM3 refused lines
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- LIST INGRE3 refused lines
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- LACKS N/C2 refused lines
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- NUTRIT LBL2 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
- INCONSPICU1 refused line
Required information not conspicuous
Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.
Questions about Haelssen & Lyon GmbH
- Is Haelssen & Lyon GmbH on an FDA import alert?
- Yes. As of October 26, 2026, Haelssen & Lyon GmbH is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for gogi berries wolfberries; FDA published the listing on December 22, 2011.
- Has FDA refused shipments from Haelssen & Lyon GmbH?
- Yes. FDA refused 3 shipment lines from Haelssen & Lyon GmbH between June 20, 2023 and July 28, 2023. The most recent, on July 28, 2023, was tea, green, charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Haelssen & Lyon GmbH's shipments?
- The most frequent charges are LACKS FIRM (manufacturer name and address missing, 3 lines) and LIST INGRE (ingredients not listed, 3 lines).
- When was Haelssen & Lyon GmbH last inspected by FDA?
- FDA's most recent inspection of Haelssen & Lyon GmbH with a final classification is dated September 19, 2024 and was classified NAI (No Action Indicated).
- What is Haelssen & Lyon GmbH's FEI number?
- Haelssen & Lyon GmbH's FDA Establishment Identifier (FEI) is 3005130014.
- Can shipments from Haelssen & Lyon GmbH still enter the U.S.?
- Shipments of gogi berries wolfberries from Haelssen & Lyon GmbH can be detained without physical examination under Import Alert 99-08; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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