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Equisalud S.L.U.

FDA import alert and refusal historyHuarte, SpainFEI 3009895647

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Example subjectEquisalud S.L.U added to Import Alert 16-129 (red list)

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As of October 26, 2026, Equisalud S.L.U. is not on any FDA import alert in SupplierRadar's records; FDA refused 49 of its shipment lines between November 28, 2016 and April 5, 2018, 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
Angelica (herbal & botanicals, not teas) · NO ENGLISH
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Equisalud S.L.U.

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

2018

  1. Import refusal
    Refused, 7 lines in one entry: Angelica (herbal & botanicals, not teas); Hawthorn (herbal & botanicals, not teas) and 3 moreNO ENGLISHNUTRIT LBLEntry 799-5015474-7Show 7 lines
    Source
  2. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ
    Source

2016

  1. Import refusal
    Refused, 42 lines in one entry: Valerian (herbal & botanicals, not teas ii); Echinacea, herbal & botanicals (not teas) and 25 moreDIRECTIONSDIETARYLBLFILTHYLACKS FIRMEntry 799-7864042-8Show 42 lines
    Source

Refusal charges, in plain English

  • NO ENGLISH49 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.

  • NUTRIT LBL48 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.

  • DIETARYLBL42 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).

  • NCONTACT42 refused lines

    No U.S. adverse event contact on supplement label

    The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

  • DIRECTIONS37 refused lines

    DIRECTIONS

  • LACKS FIRM37 refused lines

    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.

  • LIST INGRE12 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).

  • ALLERGEN6 refused lines

    Major food allergen not declared

    The label appeared not to declare all major food allergens present in the product, as section 403(w) of the FD&C Act requires.

Questions about Equisalud S.L.U.

Is Equisalud S.L.U. on an FDA import alert?
No listing for Equisalud S.L.U. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Spain page.
Has FDA refused shipments from Equisalud S.L.U.?
Yes. FDA refused 49 shipment lines from Equisalud S.L.U. between November 28, 2016 and April 5, 2018. The most recent, on April 5, 2018, was angelica (herbal & botanicals, not teas), charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Equisalud S.L.U.'s shipments?
The most frequent charges are NO ENGLISH (required label information not in english, 49 lines) and NUTRIT LBL (nutrition information missing from label, 48 lines).
When was Equisalud S.L.U. last inspected by FDA?
FDA's most recent inspection of Equisalud S.L.U. with a final classification is dated March 12, 2018 and was classified VAI (Voluntary Action Indicated).
What is Equisalud S.L.U.'s FEI number?
Equisalud S.L.U.'s FDA Establishment Identifier (FEI) is 3009895647.

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Example subjectEquisalud S.L.U 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.