Mondelez Global
FDA import alert and refusal historyParanaque, PhilippinesFEI 3004326174
As of October 25, 2026, Mondelez Global (Paranaque, Philippines) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for eden cheese, published by FDA on February 3, 2015, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-39 · red list
- Last import refusal
- Cheese and cheese products, not elsewhere mentioned, n.e.c. · LABELING
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Mondelez Global
2 records, newest first. Each line links to the FDA page it came from.
2026
2015
- Import alert listingListed on Import Alert 99-39red listEden CheeseSource
Refusal charges, in plain English
- LABELING1 refused line
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
Questions about Mondelez Global
- Is Mondelez Global on an FDA import alert?
- Yes. As of October 25, 2026, Mondelez Global is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for eden cheese; FDA published the listing on February 3, 2015.
- Has FDA refused shipments from Mondelez Global?
- Yes. FDA refused 1 shipment line from Mondelez Global on January 21, 2026. The most recent, on January 21, 2026, was cheese and cheese products, not elsewhere mentioned, n.e.c., charged as LABELING (fair packaging and labeling act).
- Why did FDA refuse Mondelez Global's shipments?
- The most frequent charge is LABELING (fair packaging and labeling act, 1 line).
- What is Mondelez Global's FEI number?
- Mondelez Global's FDA Establishment Identifier (FEI) is 3004326174.
- Can shipments from Mondelez Global still enter the U.S.?
- Shipments of eden cheese from Mondelez Global can be detained without physical examination under Import Alert 99-39; 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).
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