Lucozade Ribena Suntory Ltd

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

Refusal charges, in plain English

• UNSAFE COL5 refused lines

  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.

• LACKS FIRM2 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.

• 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.

• NUTRIT LBL1 refused line

  Nutrition information missing from label

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

• 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 Lucozade Ribena Suntory Ltd

Is Lucozade Ribena Suntory Ltd on an FDA import alert?

Yes. As of October 26, 2026, Lucozade Ribena Suntory Ltd is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for ribena blackcurrant concentrate; FDA published the listing on December 15, 2016.

Has FDA refused shipments from Lucozade Ribena Suntory Ltd?

Yes. FDA refused 8 shipment lines from Lucozade Ribena Suntory Ltd between October 5, 2016 and February 4, 2022. The most recent, on February 4, 2022, was currants, black cassis, juices or concentrates, charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Lucozade Ribena Suntory Ltd's shipments?

The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 5 lines) and LACKS FIRM (manufacturer name and address missing, 2 lines).

What is Lucozade Ribena Suntory Ltd's FEI number?

Lucozade Ribena Suntory Ltd's FDA Establishment Identifier (FEI) is 3011721955.

Can shipments from Lucozade Ribena Suntory Ltd still enter the U.S.?

Shipments of ribena blackcurrant concentrate from Lucozade Ribena Suntory Ltd 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).