Tio Francisco Queso Para Freir 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

Tio Francisco Queso Para Freir 16 oz. Tio Francisco Queso Para Freir Available to consumers at retail deli counters in various sizes Freir (bulk)

Food: Cheese

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.

All dates through 04/17/2024 Freir (bulk) PLU Batch ID 101 1EW-23312 101 1DY-23313 101 2EW-23319 101 2EW-23320 101 3EW-23325 101 3EY-23333 101 4EW-23334 101 1EX-23345 101 2DY-23354 101 1EX-23362 101 2EX-24004 101 4EW-24018 101 1EW-24026

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-0922-2024 · event 93814
Official record: FDA enforcement report search