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Wonderturn Ltd

FDA import alert and refusal historyLondon, United KingdomFEI 3003861226

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Example subjectWonderturn Lt added to Import Alert 16-129 (red list)

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As of October 25, 2026, Wonderturn Ltd (London, United Kingdom) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for luconzade energy drink; luconzade energy drink; luconzade energy drink, 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

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

Every FDA record for Wonderturn Ltd

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

2009

  1. Import alert listing
    Listed on Import Alert 45-02red listLuconzade Energy Drink; Luconzade energy drink; luconzade energy drink
    Source

Questions about Wonderturn Ltd

Is Wonderturn Ltd on an FDA import alert?
Yes. As of October 25, 2026, Wonderturn Ltd is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for luconzade energy drink; luconzade energy drink; luconzade energy drink; FDA published the listing on September 18, 2009.
Has FDA refused shipments from Wonderturn Ltd?
No FDA import refusals for Wonderturn Ltd appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is Wonderturn Ltd's FEI number?
Wonderturn Ltd's FDA Establishment Identifier (FEI) is 3003861226.
Can shipments from Wonderturn Ltd still enter the U.S.?
Shipments of luconzade energy drink; luconzade energy drink; luconzade energy drink from Wonderturn Ltd can be detained without physical examination under Import Alert 45-02; 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 subjectWonderturn Lt 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.