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Nordee Irlande

FDA import alert and refusal historyPort Of Prince, HaitiFEI 3031569423

Recorded by FDA as NORDEE IRLANDE

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

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As of October 25, 2026, Nordee Irlande is not on any FDA import alert in SupplierRadar's records; FDA refused 7 of its shipment lines on August 20, 2024, most often for required label information not in english (NO ENGLISH).

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

Current status

Import alerts
Not listed
Last import refusal
Infant formula raw material component, n.e.c., · DIETARYLBL
Last warning letter
None found
Last inspection
None on record

Every FDA record for Nordee Irlande

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

2024

  1. Import refusal
    Refused, 7 lines in one entry: Infant formula raw material component, n.e.c.,; Vitamin c (ascorbic acid) and 2 moreDIETARYLBLLACKS N/CNUTRIT LBLNO ENGLISHEntry 9UA-0308895-4Show 7 lines
    Source

Refusal charges, in plain English

  • NO ENGLISH5 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

  • DIETARYLBL4 refused lines

    Not identified as a dietary supplement

    The label appeared not to identify the product with the term "dietary supplement" (which may be modified with the name of an ingredient).

  • NUTRIT LBL4 refused lines

    Nutrition information missing from label

    The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

  • LACKS N/C1 refused line

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

Questions about Nordee Irlande

Is Nordee Irlande on an FDA import alert?
No listing for Nordee Irlande appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Haiti page.
Has FDA refused shipments from Nordee Irlande?
Yes. FDA refused 7 shipment lines from Nordee Irlande on August 20, 2024. The most recent, on August 20, 2024, was infant formula raw material component, n.e.c.,, charged as DIETARYLBL (not identified as a dietary supplement).
Why did FDA refuse Nordee Irlande's shipments?
The most frequent charges are NO ENGLISH (required label information not in english, 5 lines) and DIETARYLBL (not identified as a dietary supplement, 4 lines).
What is Nordee Irlande's FEI number?
Nordee Irlande's FDA Establishment Identifier (FEI) is 3031569423.

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Example subjectNordee Irland 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.