Tio Francisco Blanco Suave 14 oz. UPC 7-27242-05355-6
Summary
The FDA issued a Class I for Tio Francisco Blanco Suave 14 oz. UPC 7-27242-05355-6 by Rizo Lopez Foods, Inc. dba Don Francisco Cheese. Reason: Listeria monocytogenes contamination..
Details
Source
Food Recall
External ID
F-0917-2024
Action Date
2024-02-07
Status
Ongoing
Category
food
Product Description
Tio Francisco Blanco Suave 14 oz. UPC 7-27242-05355-6
Lot/Code Info: All dates through 03/23/2024
Reason for Recall
Listeria monocytogenes contamination.
Distribution
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-01-11
Company
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Rizo Lopez Foods, Inc. dba Don Francisco Cheese has 14 FDA actions in our database, including 14 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Rizo Lopez Foods, Inc. dba Don Francisco Cheese) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Rizo Lopez Foods, Inc. dba Don Francisco Cheese have FDA actions?
Rizo Lopez Foods, Inc. dba Don Francisco Cheese has 14 FDA actions in our database, including 14 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0917-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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