RecallHawk
Class I Recall

Cricket Creek Farm brand Sophelise cheese

Cricket Creek Farm LLC

Summary

The FDA issued a Class I for Cricket Creek Farm brand Sophelise cheese by Cricket Creek Farm LLC. Reason: Products may be contaminated with Listeria monocytogenes..

Details

Source

Food Recall

External ID

F-1022-2023

Action Date

2023-07-12

Status

Terminated

Category

food

Product Description

Cricket Creek Farm brand Sophelise cheese

Lot/Code Info: Batch #055 Produced Feb 24, 2023 Distributed between March 29, 2023 to May 21, 2023

Quantity Affected: 165 units

Reason for Recall

Products may be contaminated with Listeria monocytogenes.

Distribution

NY, MA, CT

Type: Voluntary: Firm initiated

Recall Initiated: 2023-05-25

Company

Cricket Creek Farm LLC

Williamstown, MA

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 228 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Cricket Creek Farm LLC has 4 FDA actions in our database, including 4 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 (Cricket Creek Farm LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Cricket Creek Farm LLC have FDA actions?

Cricket Creek Farm LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1022-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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