RecallHawk
Class I Recall

Cahill Whiskey Cheddar Cheese packaged in clear plastic PLU 5478494884

Whole Foods Market

Summary

The FDA issued a Class I for Cahill Whiskey Cheddar Cheese packaged in clear plastic PLU 5478494884 by Whole Foods Market. Reason: Potential to be contaminated with Listeria monocytogenes.

Details

Source

Food Recall

External ID

F-0902-2021

Action Date

2021-09-08

Status

Terminated

Category

food

Product Description

Cahill Whiskey Cheddar Cheese packaged in clear plastic PLU 5478494884

Lot/Code Info: May 17 - July 26, 2021

Quantity Affected: 18.64 lbs

Reason for Recall

Potential to be contaminated with Listeria monocytogenes

Distribution

Alabama, Arkansas, California, Colorado, Florida, Hawaii, Illinois, Indiana, Iowa, Louisiana, Michigan, Mississippi, Missouri, Nebraska, Nevada, New Hampshire, New York, North Carolina, Oklahoma, Texas, Wisconsin, Wyoming

Type: Voluntary: Firm initiated

Recall Initiated: 2021-07-27

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

Whole Foods Market 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 (Whole Foods Market) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Whole Foods Market have FDA actions?

Whole Foods Market 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-0902-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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