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Penwarden Holdings (N.Z.) Ltd.

FDA import alert and refusal historyAukland, New ZealandFEI 1000145353

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Example subjectPenwarden Holdings (N.Z.) Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Penwarden Holdings (N.Z.) Ltd. (Aukland, New Zealand) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for lobster tails, published by FDA on September 16, 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 Penwarden Holdings (N.Z.) Ltd.

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

2009

  1. Import alert listing
    Listed on Import Alert 99-21red listLobster Tails
    Source

Questions about Penwarden Holdings (N.Z.) Ltd.

Is Penwarden Holdings (N.Z.) Ltd. on an FDA import alert?
Yes. As of October 26, 2026, Penwarden Holdings (N.Z.) Ltd. is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for lobster tails; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Penwarden Holdings (N.Z.) Ltd.?
No FDA import refusals for Penwarden Holdings (N.Z.) Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Penwarden Holdings (N.Z.) Ltd.'s FEI number?
Penwarden Holdings (N.Z.) Ltd.'s FDA Establishment Identifier (FEI) is 1000145353.
Can shipments from Penwarden Holdings (N.Z.) Ltd. still enter the U.S.?
Shipments of lobster tails from Penwarden Holdings (N.Z.) Ltd. can be detained without physical examination under Import Alert 99-21; 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 subjectPenwarden Holdings (N.Z.) Ltd 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.