Jureidini'S Limited

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

Refusal charges, in plain English

• COLOR LBLG3 refused lines

  Artificial coloring not declared

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

• UNSAFE COL3 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.

Questions about Jureidini'S Limited

Is Jureidini'S Limited on an FDA import alert?

Yes. As of October 26, 2026, Jureidini'S Limited is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for anchor lemon/lime syrup; anchor orange syrup; anchor mango syrup; anchor ginger syrup; strawberry flavored syrup; FDA published the listing on February 14, 2011.

Has FDA refused shipments from Jureidini'S Limited?

Yes. FDA refused 3 shipment lines from Jureidini'S Limited between February 21, 2020 and January 14, 2022. The most recent, on January 14, 2022, was syrups and molasses, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Jureidini'S Limited's shipments?

The most frequent charges are COLOR LBLG (artificial coloring not declared, 3 lines) and UNSAFE COL (color additive unsafe under section 721, 3 lines).

When was Jureidini'S Limited last inspected by FDA?

FDA's most recent inspection of Jureidini'S Limited with a final classification is dated May 24, 2013 and was classified VAI (Voluntary Action Indicated).

What is Jureidini'S Limited's FEI number?

Jureidini'S Limited's FDA Establishment Identifier (FEI) is 3004262806.

Can shipments from Jureidini'S Limited still enter the U.S.?

Shipments of anchor lemon/lime syrup; anchor orange syrup; anchor mango syrup; anchor ginger syrup; strawberry flavored syrup from Jureidini'S Limited 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).