Refresco Benelux BV

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

Refusal charges, in plain English

• NO ENGLISH6 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.

• LACKS N/C5 refused lines

  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.

• NUTRIT LBL5 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 FIRM3 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 INGRE2 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).

• COLORLABEL1 refused line

  Required information not prominent

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

• NO PROCESS1 refused line

  No scheduled process filed

  The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

• UNSAFE COL1 refused line

  Color additive unsafe under section 721

  The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

Questions about Refresco Benelux BV

Is Refresco Benelux BV on an FDA import alert?

No listing for Refresco Benelux BV appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Netherlands page.

Has FDA refused shipments from Refresco Benelux BV?

Yes. FDA refused 10 shipment lines from Refresco Benelux BV between September 4, 2019 and December 20, 2024. The most recent, on December 20, 2024, was soft drink, other fruit flavored, carbonated, charged as LACKS N/C (net quantity statement missing).

Why did FDA refuse Refresco Benelux BV's shipments?

The most frequent charges are NO ENGLISH (required label information not in english, 6 lines) and LACKS N/C (net quantity statement missing, 5 lines).

When was Refresco Benelux BV last inspected by FDA?

FDA's most recent inspection of Refresco Benelux BV with a final classification is dated August 26, 2026 and was classified NAI (No Action Indicated).

What is Refresco Benelux BV's FEI number?

Refresco Benelux BV's FDA Establishment Identifier (FEI) is 3015157619.