Food Recall Check
Class I · High risk Terminated Initiated May 3, 2024 (2 years ago)

Cre-90 (ro1) recall

Recalled by Danisco USA Inc. · New Century, KS, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Potential Salmonella Contamination

Pathogen: Salmonella

Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

CRE-90 (RO1) 25 KG Bag Lala, 25 kg / 55.12 lb bag

Quantity: 500.00 kg

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot numbesr: 1204607206; 1204607209; 1204607211; 1204607212; 1204610370; 1204610370; 1204610373; 1204610374; 1204610377

Where it was sold

Arizona California Colorado Florida Iowa Idaho Illinois Indiana Kansas Kentucky Michigan Minnesota Missouri Nebraska New Jersey New York Ohio Oklahoma Pennsylvania Tennessee Texas Utah Virginia Wisconsin

FDA's distribution note: US: AZ, CA, CO, FL, IA, ID, IL, IN, KS, KY, MI, MN, MO, NE, NJ, NY, OH, OK, PA, TN, TX, UT, VA, WI; Canada, and Mexico

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Danisco USA Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
May 3, 2024
In FDA report of
Jun 12, 2024
Terminated
Sep 4, 2024
FDA recall number
F-1332-2024 · event 94565
Official record
FDA enforcement report search

Also recalled with it (35 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Showing 12 of 35.