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Freezitt

FDA import alert and refusal historyIttervoort, NetherlandsFEI 2000014251

Recorded by FDA as FREEZITT

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

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As of October 25, 2026, Freezitt is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between March 20, 2018 and April 16, 2018, most often for listeria monocytogenes (LISTERIA).

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

Current status

Import alerts
Not listed
Last import refusal
Mushroom, common (agaricus bisporus), pieces and stems, sliced · LISTERIA
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Freezitt

3 records, newest first. Each line links to the FDA page it came from.

2018

  1. Import refusal
    Refused, Mushroom, common (agaricus bisporus), pieces and stems, slicedLISTERIAEntry 113-8281151-8
    Source
  2. Import refusal
    Refused, Mushroom, common (agaricus bisporus), pieces and stems, slicedLISTERIAEntry 113-8258209-3
    Source

2017

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

Refusal charges, in plain English

  • LISTERIA2 refused lines

    Listeria monocytogenes

    The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.

Questions about Freezitt

Is Freezitt on an FDA import alert?
No listing for Freezitt appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.
Has FDA refused shipments from Freezitt?
Yes. FDA refused 2 shipment lines from Freezitt between March 20, 2018 and April 16, 2018. The most recent, on April 16, 2018, was mushroom, common (agaricus bisporus), pieces and stems, sliced, charged as LISTERIA (listeria monocytogenes).
Why did FDA refuse Freezitt's shipments?
The most frequent charge is LISTERIA (listeria monocytogenes, 2 lines).
When was Freezitt last inspected by FDA?
FDA's most recent inspection of Freezitt with a final classification is dated September 19, 2017 and was classified NAI (No Action Indicated).
What is Freezitt's FEI number?
Freezitt's FDA Establishment Identifier (FEI) is 2000014251.

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Example subjectFreezit 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.