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Doornfontein Hoodia Farm

FDA import alert and refusal historyCape Town, South AfricaFEI 3006416715

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Example subjectDoornfontein Hoodia Far added to Import Alert 16-129 (red list)

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As of October 26, 2026, Doornfontein Hoodia Farm (Cape Town, South Africa) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for hoodia gordonii powder, published by FDA on October 27, 2009, 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 Doornfontein Hoodia Farm

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

2009

  1. Import alert listing
    Listed on Import Alert 99-08red listHoodia Gordonii Powder
    Source

Questions about Doornfontein Hoodia Farm

Is Doornfontein Hoodia Farm on an FDA import alert?
Yes. As of October 26, 2026, Doornfontein Hoodia Farm is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for hoodia gordonii powder; FDA published the listing on October 27, 2009.
Has FDA refused shipments from Doornfontein Hoodia Farm?
No FDA import refusals for Doornfontein Hoodia Farm appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Doornfontein Hoodia Farm's FEI number?
Doornfontein Hoodia Farm's FDA Establishment Identifier (FEI) is 3006416715.
Can shipments from Doornfontein Hoodia Farm still enter the U.S.?
Shipments of hoodia gordonii powder from Doornfontein Hoodia Farm can be detained without physical examination under Import Alert 99-08; 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 subjectDoornfontein Hoodia Far 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.