Wisdom Herbs Enterprise
FDA import alert and refusal historyGeorgetown, MalaysiaFEI 3007016727
As of October 26, 2026, Wisdom Herbs Enterprise (Georgetown, Malaysia) is on the red list of FDA Import Alert 54-15 (Supplements and ingredients containing kratom) for uncaria gembier; kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii), 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 Wisdom Herbs Enterprise
1 record, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 54-15red listUncaria Gembier; Kratom (Herbal and Botanical Teas II, continued); Kratom (Herbal and Botanicals, not Teas II)Source
Questions about Wisdom Herbs Enterprise
- Is Wisdom Herbs Enterprise on an FDA import alert?
- Yes. As of October 26, 2026, Wisdom Herbs Enterprise is on the red list of FDA Import Alert 54-15, “Supplements and ingredients containing kratom”, for uncaria gembier; kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii); FDA published the listing on February 28, 2014.
- Has FDA refused shipments from Wisdom Herbs Enterprise?
- No FDA import refusals for Wisdom Herbs Enterprise appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Wisdom Herbs Enterprise's FEI number?
- Wisdom Herbs Enterprise's FDA Establishment Identifier (FEI) is 3007016727.
- Can shipments from Wisdom Herbs Enterprise still enter the U.S.?
- Shipments of uncaria gembier; kratom (herbal and botanical teas ii, continued); kratom (herbal and botanicals, not teas ii) from Wisdom Herbs Enterprise 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.