Laboratoire Manuves
FDA import alert and refusal historyPointe-claire, CanadaFEI 3006603941
As of October 26, 2026, Laboratoire Manuves (Pointe-claire, Canada) is on the red list of FDA Import Alert 45-06 (Stevia leaves, crude extracts and foods containing them) for fenugreek (herbal & botanicals, not teas); anti-diabetic n.e.c., human - non/rx combination ingredient, nonsterile liquid, published by FDA on September 18, 2009, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-06 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Laboratoire Manuves
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-06red listFenugreek (Herbal & Botanicals, not Teas); Anti-Diabetic N.E.C., Human - Non/Rx Combination Ingredient, NonSterile LiquidSource
Questions about Laboratoire Manuves
- Is Laboratoire Manuves on an FDA import alert?
- Yes. As of October 26, 2026, Laboratoire Manuves is on the red list of FDA Import Alert 45-06, “Stevia leaves, crude extracts and foods containing them”, for fenugreek (herbal & botanicals, not teas); anti-diabetic n.e.c., human - non/rx combination ingredient, nonsterile liquid; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Laboratoire Manuves?
- No FDA import refusals for Laboratoire Manuves appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Laboratoire Manuves's FEI number?
- Laboratoire Manuves's FDA Establishment Identifier (FEI) is 3006603941.
- Can shipments from Laboratoire Manuves still enter the U.S.?
- Shipments of fenugreek (herbal & botanicals, not teas); anti-diabetic n.e.c., human - non/rx combination ingredient, nonsterile liquid from Laboratoire Manuves can be detained without physical examination under Import Alert 45-06; 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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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.