Mondelez Global Llc Recall: Mondelez Global received notification from a supplier, Associated Milk Producers, Inc. ( AMPI ), of a voluntary recall of Whey Powder Sweet Type as a precautionary measure due to the potential presence of Salmonella. The recalled whey powder is used as an ingredient in various Mondelez Global human food products.

🇺🇸 United States

1. July 21, 2018 - Recall initiated
2. August 8, 2018 - Reported by source
3. March 27, 2023 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1782-2018

Event ID

80616

Status

Terminated

Classification

Class II

Company

Mondelez Global Llc

Product description

10.8Z RITZ BACON AND CHEESE 14,(9 & 14) 10.8 Oz per tray, Plastic sleeve in tray 14 trays per case

Quantity

162 Cases

Reason

Mondelez Global received notification from a supplier, Associated Milk Producers, Inc. ( AMPI ), of a voluntary recall of Whey Powder Sweet Type as a precautionary measure due to the potential presence of Salmonella. The recalled whey powder is used as an ingredient in various Mondelez Global human food products.

Recall initiation date

July 21, 2018

Report date

August 8, 2018

Classification date

Not published in this source record

Termination date

March 27, 2023

Distribution pattern

The impacted products were shipped to Consignees in the U.S., including Puerto Rico & the U.S. Virgin Islands. They were also shipped to consignees in Anguilla, Antigua/Barbuda, Aruba, Barbados, Belize, Bermuda, Costa Rica, Curacao, Guatemala, Jamaica, Panama, Philippines, St. Eustatius, St. Vincent, Suriname and Trinidad. Please see attached spreadsheets for number of Domestic Consigne

UPC, lot, and code information

0 44000 04566 1 0 44000 04567 8

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

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 80616 with 9 other product entries in Public Health Trace.

Responsible company: Mondelez Global Llc

Other recalls from Mondelez Global Llc

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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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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