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K.Paulsen Botanicals

FDA import alert and refusal historySwellendam, South AfricaFEI 3011558115

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Example subjectK.Paulsen Botanical added to Import Alert 16-129 (red list)

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As of October 25, 2026, K.Paulsen Botanicals (Swellendam, South Africa) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for organic moringa leaf powder, published by FDA on March 16, 2016, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for K.Paulsen Botanicals

1 record, newest first. Each line links to the FDA page it came from.

2016

  1. Import alert listing
    Listed on Import Alert 99-19red listOrganic Moringa Leaf Powder
    Source

Questions about K.Paulsen Botanicals

Is K.Paulsen Botanicals on an FDA import alert?
Yes. As of October 25, 2026, K.Paulsen Botanicals is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for organic moringa leaf powder; FDA published the listing on March 16, 2016.
Has FDA refused shipments from K.Paulsen Botanicals?
No FDA import refusals for K.Paulsen Botanicals appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is K.Paulsen Botanicals's FEI number?
K.Paulsen Botanicals's FDA Establishment Identifier (FEI) is 3011558115.
Can shipments from K.Paulsen Botanicals still enter the U.S.?
Shipments of organic moringa leaf powder from K.Paulsen Botanicals can be detained without physical examination under Import Alert 99-19; 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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Example subjectK.Paulsen Botanical added to Import Alert 16-129 (red list)

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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.