FDA recall record

Mondelez Global 1Z RITZ BITS CHEESE 120 1 Oz Pouches recall — FDA F-1779-2018

Mondelez Global received notification from a supplier, Associated Milk Producers, Inc. ( AMPI ), of a voluntary recall of Whey Powder Sweet Type as a…

Class IIclassification
F-1779-2018official record ID
Aug 8, 2018report date

Recall record at a glance

Official recordF-1779-2018
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMondelez Global LLC
Report dateAug 8, 2018
Recall initiation dateJul 21, 2018
Quantity3,375 Cases
LocationEast Hanover, NJ, United States

Official product description

1Z RITZ BITS CHEESE 120 1 Oz Pouches

Why the product was recalled

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.

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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