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Genex Nutraceuticals

FDA import alert and refusal historyConcord, CanadaFEI 3016418013

Recorded by FDA as GENEX NUTRACEUTICALS

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

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As of October 26, 2026, Genex Nutraceuticals is not on any FDA import alert in SupplierRadar's records; FDA refused 32 of its shipment lines between July 11, 2024 and August 6, 2024, 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
Whey protein powder (vit/min/protein/unconventional dietary spec for human/animal, n.e.c.) · LIST INGRE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Genex Nutraceuticals

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

2024

  1. Import refusal
    Refused, 10 lines in one entry: Whey protein powder (vit/min/protein/unconventional dietary spec for human/animal, n.e.c.)LIST INGREINCONSPICUNUTRIT LBLCOLOR LBLGEntry EI5-2439506-5Show 10 lines
    Source
  2. Import refusal
    Refused, 22 lines in one entry: Whey protein powder (vit/min/protein/unconventional dietary spec for human/animal, n.e.c.); Foods with supplemental nutrients added, with or without artifical sweetnersLIST INGREUNSAFE ADDCOLOR LBLGNUTRIT LBLEntry EI5-2437725-3Show 22 lines
    Source

Refusal charges, in plain English

  • LIST INGRE31 refused lines

    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).

  • NUTRIT LBL31 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.

  • COLOR LBLG13 refused lines

    Artificial coloring not declared

    The product appeared to contain an artificial coloring without labeling that states that fact.

  • UNSAFE ADD12 refused lines

    Food additive unsafe under section 409

    The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

  • INCONSPICU10 refused lines

    Required information not conspicuous

    Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.

  • FALSE1 refused line

    False or misleading labeling

    The labeling appeared to be false or misleading in some particular.

  • LACKS FIRM1 refused line

    Manufacturer name and address missing

    The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

  • USUAL NAME1 refused line

    Common or usual name missing

    The label appeared not to show the common or usual name of the food.

Questions about Genex Nutraceuticals

Is Genex Nutraceuticals on an FDA import alert?
No listing for Genex Nutraceuticals appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Canada page.
Has FDA refused shipments from Genex Nutraceuticals?
Yes. FDA refused 32 shipment lines from Genex Nutraceuticals between July 11, 2024 and August 6, 2024. The most recent, on August 6, 2024, was whey protein powder (vit/min/protein/unconventional dietary spec for human/animal, n.e.c.), charged as LIST INGRE (ingredients not listed).
Why did FDA refuse Genex Nutraceuticals's shipments?
The most frequent charges are LIST INGRE (ingredients not listed, 31 lines) and NUTRIT LBL (nutrition information missing from label, 31 lines).
What is Genex Nutraceuticals's FEI number?
Genex Nutraceuticals's FDA Establishment Identifier (FEI) is 3016418013.

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Example subjectGenex Nutraceutical 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.