Queso de mano, Fresh soft white cheese, NET WT 24 oz.(640g), Keep Refrigerated, plastic container, packed 12 plastic co
Summary
The FDA issued a Class I for Queso de mano, Fresh soft white cheese, NET WT 24 oz.(640g), Keep Refrigerated, by Tama Corporation. Reason: Potential contamination with Listeria Monocytogenes.
Details
Source
Food Recall
External ID
F-1262-2024
Action Date
2024-05-29
Status
Terminated
Category
food
Product Description
Queso de mano, Fresh soft white cheese, NET WT 24 oz.(640g), Keep Refrigerated, plastic container, packed 12 plastic containers of 24 oz per case
Lot/Code Info: Lot# L2420104 UPC barcode: 838795000338 Expiration date: May 16th, 2024
Quantity Affected: 216 units = 18 cases
Reason for Recall
Potential contamination with Listeria Monocytogenes
Distribution
The product has been distributed in the following State: UT
Type: Voluntary: Firm initiated
Recall Initiated: 2024-04-24
Company
Doral, FL
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 27 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Tama Corporation has 2 FDA actions in our database, including 2 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 (Tama Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Tama Corporation have FDA actions?
Tama Corporation has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1262-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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