Mondelez Global, LLC

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

Refusal charges, in plain English

• NO ENGLISH3 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.

• LIST INGRE1 refused line

  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).

• UNAPPROVED1 refused line

  Unapproved new drug

  The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Mondelez Global, LLC

Is Mondelez Global, LLC on an FDA import alert?

No listing for Mondelez Global, LLC appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Turkey page.

Has FDA refused shipments from Mondelez Global, LLC?

Yes. FDA refused 3 shipment lines from Mondelez Global, LLC between May 19, 2017 and December 20, 2024. The most recent, on December 20, 2024, was candy specialties, n.e.c. (without chocolate), charged as NO ENGLISH (required label information not in english).

Why did FDA refuse Mondelez Global, LLC's shipments?

The most frequent charges are NO ENGLISH (required label information not in english, 3 lines) and LIST INGRE (ingredients not listed, 1 line).

When was Mondelez Global, LLC last inspected by FDA?

FDA's most recent inspection of Mondelez Global, LLC with a final classification is dated May 21, 2024 and was classified NAI (No Action Indicated).

What is Mondelez Global, LLC's FEI number?

Mondelez Global, LLC's FDA Establishment Identifier (FEI) is 3009488958.