Monterey Jack Conventional recall

Recalled by Rizo Lopez Foods, Inc. dba Don Francisco Cheese · Modesto, CA, United States

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

Why it was recalled

Listeria monocytogenes contamination.

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

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

Monterey Jack Conventional (bulk)

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.

PLU Batch ID 40200 1DZ-23249 40200 2DY-23249 40200 3DX-23249 40200 4CW-23249 40200 1DY-23279 40200 2DX-23279 40200 3CW-23279 40200 4CZ-23279 40200 1DZ-23283 40200 2DY-23283 40200 3CW-23283 40200 4CZ-23283 40200 2EY-23284 40200 3EX-23284 40200 4EW-23284 40200 1EX-23314 40200 2DW-23314 40200 3DZ-23314 40200 4DY-23314 40200 1DZ-24019 40200 2EY-24019 40200 3EX-24019 40200 4EW-24019 40200 1CY-24027 40200 2DX-24027 40200 3DW-24027 40200 4DZ-24027

Where it was sold

Arkansas Arizona California Colorado Florida Georgia Iowa Illinois Kansas Maryland North Carolina New Jersey Nevada New York Oregon Rhode Island Texas Utah Virginia Washington

FDA's distribution note: U.S. distribution to the following: AR, AZ, BC, CA, CO, FL, GA, IA, IL, KS, MD, NC,NJ, NV, NY, OR, RI, TX, UT, VA, WA, W No foreign distribution.

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.

Recalling firm: Rizo Lopez Foods, Inc. dba Don Francisco Cheese
Initiated by: Voluntary: Firm initiated
Recall initiated: Jan 11, 2024
In FDA report of: Feb 7, 2024
FDA recall number: F-0928-2024 · event 93814
Official record: FDA enforcement report search