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Mondelez Ireland

FDA import alert and refusal historyDublin 17, IrelandFEI 3012464098

Recorded by FDA as MONDELEZ IRELAND

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

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As of October 26, 2026, Mondelez Ireland is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on May 2, 2018, most often for ingredients not listed (LIST INGRE).

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

Current status

Import alerts
Not listed
Last import refusal
Chocolate candy bar, without nuts and fruit · LIST INGRE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Mondelez Ireland

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

2018

  1. Import refusal
    Refused, Chocolate candy bar, without nuts and fruitLIST INGREEntry KM6-3513180-8
    Source

Refusal charges, in plain English

  • LIST INGRE1 refused line

    Ingredients not listed

    The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

Questions about Mondelez Ireland

Is Mondelez Ireland on an FDA import alert?
No listing for Mondelez Ireland appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Ireland page.
Has FDA refused shipments from Mondelez Ireland?
Yes. FDA refused 1 shipment line from Mondelez Ireland on May 2, 2018. The most recent, on May 2, 2018, was chocolate candy bar, without nuts and fruit, charged as LIST INGRE (ingredients not listed).
Why did FDA refuse Mondelez Ireland's shipments?
The most frequent charge is LIST INGRE (ingredients not listed, 1 line).
What is Mondelez Ireland's FEI number?
Mondelez Ireland's FDA Establishment Identifier (FEI) is 3012464098.

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Example subjectMondelez Irelan 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.