Lustrel Laboratoires SAS
FDA import alert and refusal historySaint-jean-de-vedas, FranceFEI 3012325316
As of October 26, 2026, Lustrel Laboratoires SAS is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on December 21, 2017, most often for not identified as a dietary supplement (DIETARYLBL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Foods with supplemental nutrients added, with or without artifical sweetners · LIST INGRE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Lustrel Laboratoires SAS
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import refusalSource
Refused, 2 lines in one entry: Foods with supplemental nutrients added, with or without artifical sweetnersLIST INGREDIETARYLBLFALSELACKS FIRMEntry UPS-4890409-9Show 2 linesHide lines
- Refused, Foods with supplemental nutrients added, with or without artifical sweetnersLIST INGREDIETARYLBLFALSELACKS FIRMLACKS N/CNUTRIT LBLEntry UPS-4890409-9Source
- Refused, Foods with supplemental nutrients added, with or without artifical sweetnersLIST INGREDIETARYLBLLACKS FIRMLACKS N/CUSUAL NAMEALLERGENNUTRIT LBLEntry UPS-4890409-9Source
Refusal charges, in plain English
- DIETARYLBL2 refused lines
Not identified as a dietary supplement
The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).
- LACKS FIRM2 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.
- 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.
- LIST INGRE2 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).
- 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.
- ALLERGEN1 refused line
Major food allergen not declared
The label appeared not to declare all major food allergens present in the product, as section 403(w) of the FD&C Act requires.
- FALSE1 refused line
False or misleading labeling
The labeling appeared to be false or misleading in some particular.
- USUAL NAME1 refused line
Common or usual name missing
The label appeared not to show the common or usual name of the food.
Questions about Lustrel Laboratoires SAS
- Is Lustrel Laboratoires SAS on an FDA import alert?
- No listing for Lustrel Laboratoires SAS appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the France page.
- Has FDA refused shipments from Lustrel Laboratoires SAS?
- Yes. FDA refused 2 shipment lines from Lustrel Laboratoires SAS on December 21, 2017. The most recent, on December 21, 2017, was foods with supplemental nutrients added, with or without artifical sweetners, charged as LIST INGRE (ingredients not listed).
- Why did FDA refuse Lustrel Laboratoires SAS's shipments?
- The most frequent charges are DIETARYLBL (not identified as a dietary supplement, 2 lines) and LACKS FIRM (manufacturer name and address missing, 2 lines).
- What is Lustrel Laboratoires SAS's FEI number?
- Lustrel Laboratoires SAS's FDA Establishment Identifier (FEI) is 3012325316.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.