RecallHawk
Class I Recall

Queso de mano, Fresh soft white cheese, NET WT 24 oz.(640g), Keep Refrigerated, plastic container, packed 12 plastic co

Tama Corporation

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

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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