Mondelez International Recall: Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and mint varieties) due to milk allergen not being declared on the ingredient list.

🇺🇸 United States

1. October 28, 2016 - Recall initiated
2. December 14, 2016 - Reported by source
3. May 22, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0671-2017

Event ID

75574

Status

Terminated

Classification

Class I

Company

Mondelez International

Product description

Nabisco Oreo Fudge Creme Original Variety, Net Wt. 11.3 oz Distributed by: Mondelez Global LLC East Hanover, NJ UPC 044000026943

Quantity

unknown

Reason

Mondelez Global LLC is recalling certain Oreo Fudge Cremes (Original and mint varieties) due to milk allergen not being declared on the ingredient list.

Recall initiation date

October 28, 2016

Report date

December 14, 2016

Classification date

Not published in this source record

Termination date

May 22, 2018

Distribution pattern

Nationwide, PR, St. Croix and St. Thomas Phillipines

UPC, lot, and code information

UPC 044000026943; 19 AUG 16 20 Aug 16 14 SEP 16 13 OCT 16 14 OCT 16 17 OCT 16

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 75574 with 1 other product entry in Public Health Trace.

Responsible company: Mondelez International

Other recalls from Mondelez International

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Puerto Rico	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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