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Nordcom Group AB

FDA import alert and refusal historyGoteborg, SwedenFEI 3033273704

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Example subjectNordcom Group A added to Import Alert 16-129 (red list)

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As of October 26, 2026, Nordcom Group AB (Goteborg, Sweden) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for bubs bubblegum skalle; bubs lemon raspberry skalle; banana bubs, published by FDA on March 9, 2026, 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 Nordcom Group AB

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

2026

  1. Import alert listing
    Listed on Import Alert 45-02red listBUBS Bubblegum SKALLE; BUBS Lemon Raspberry SKALLE; Banana Bubs
    Source

Questions about Nordcom Group AB

Is Nordcom Group AB on an FDA import alert?
Yes. As of October 26, 2026, Nordcom Group AB is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for bubs bubblegum skalle; bubs lemon raspberry skalle; banana bubs; FDA published the listing on March 9, 2026.
Has FDA refused shipments from Nordcom Group AB?
No FDA import refusals for Nordcom Group AB appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Nordcom Group AB's FEI number?
Nordcom Group AB's FDA Establishment Identifier (FEI) is 3033273704.
Can shipments from Nordcom Group AB still enter the U.S.?
Shipments of bubs bubblegum skalle; bubs lemon raspberry skalle; banana bubs from Nordcom Group AB 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 subjectNordcom Group A 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.