Three Ocean Export
FDA import alert and refusal historyNorth Vancouver, CanadaFEI 3010107627
As of October 26, 2026, Three Ocean Export (North Vancouver, Canada) is on the red list of FDA Import Alert 54-15 (Supplements and ingredients containing kratom) for kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii); mitragyna speciosa dried leaf, published by FDA on February 28, 2014, 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 54-15 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Three Ocean Export
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 54-15red listKratom (Herbal and Botanical Teas II, continued); Kratom (Herbal and Botanicals, not Teas II); Mitragyna Speciosa Dried LeafSource
Questions about Three Ocean Export
- Is Three Ocean Export on an FDA import alert?
- Yes. As of October 26, 2026, Three Ocean Export is on the red list of FDA Import Alert 54-15, “Supplements and ingredients containing kratom”, for kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii); mitragyna speciosa dried leaf; FDA published the listing on February 28, 2014.
- Has FDA refused shipments from Three Ocean Export?
- No FDA import refusals for Three Ocean Export appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Three Ocean Export's FEI number?
- Three Ocean Export's FDA Establishment Identifier (FEI) is 3010107627.
- Can shipments from Three Ocean Export still enter the U.S.?
- Shipments of kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii); mitragyna speciosa dried leaf from Three Ocean Export can be detained without physical examination under Import Alert 54-15; 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.