RecallHawk
Class I Recall

Aged raw milk cheese "Wallaby" 4 oz to 12 oz packages

Keswick Creamery at Carrock Farms LLC

Summary

The FDA issued a Class I for Aged raw milk cheese "Wallaby" 4 oz to 12 oz packages by Keswick Creamery at Carrock Farms LLC. Reason: All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes..

Details

Source

Food Recall

External ID

F-1797-2022

Action Date

2022-10-05

Status

Terminated

Category

food

Product Description

Aged raw milk cheese "Wallaby" 4 oz to 12 oz packages

Lot/Code Info: Batch 27

Quantity Affected: 46 lbs

Reason for Recall

All products manufactured by the firm have the potential to be contaminated with Listeria monocytogenes.

Distribution

Distributed to farm stores and farmers markets in Washington DC, MD, VA, and PA

Type: Voluntary: Firm initiated

Recall Initiated: 2022-08-25

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

Keswick Creamery at Carrock Farms LLC has 10 FDA actions in our database, including 10 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 (Keswick Creamery at Carrock Farms LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Keswick Creamery at Carrock Farms LLC have FDA actions?

Keswick Creamery at Carrock Farms LLC has 10 FDA actions in our database, including 10 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1797-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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