RecallHawk
Class I Recall

1. Cahills Ireland Original Irish Porter 5lbs.Waxed Deli Wheel 2. Cahills Ireland Original Irish Porter 2.4 lbs.

CAHILLS FARM CHEESE LIMITED

Summary

The FDA issued a Class I for 1. Cahills Ireland Original Irish Porter 5lbs.Waxed Deli Wheel 2. Cahills Irela by CAHILLS FARM CHEESE LIMITED. Reason: Cheese may be contaminated with Listeria monocytogenes..

Details

Source

Food Recall

External ID

F-0881-2021

Action Date

2021-09-01

Status

Terminated

Category

food

Product Description

1. Cahills Ireland Original Irish Porter 5lbs.Waxed Deli Wheel 2. Cahills Ireland Original Irish Porter 2.4 lbs.

Lot/Code Info: Batch 21109 Bath 21141 1. UPC Codes: 833334009940 2.UPC Codes: 034463012201

Quantity Affected: 4.4 tons (total)

Reason for Recall

Cheese may be contaminated with Listeria monocytogenes.

Distribution

nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2021-07-26

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

CAHILLS FARM CHEESE LIMITED has 5 FDA actions in our database, including 5 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 (CAHILLS FARM CHEESE LIMITED) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does CAHILLS FARM CHEESE LIMITED have FDA actions?

CAHILLS FARM CHEESE LIMITED has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0881-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions