The Recall Desk
Agency classClass IOur severity:SevereFDA (Food)·F-0443-2017·Announced 2016-12-07

Kuster's Recalls Pepper Jack Cheese Due to Listeria Risk

Kuster's Inc. is voluntarily recalling 363 lbs of Pepper Jack cut cheese due to potential Listeria monocytogenes contamination or inadequate pasteurization.

The agency’s classification

FDA (Food): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classification is FDA Class I, which mandates a minimum severity score of 4 according to the rubric. Additionally, Listeria monocytogenes is a high-risk pathogen.

Plain-English summary

Kuster's Inc. is voluntarily recalling its shredded, sliced, and cubed cheese products, specifically A New Dairy Pepper Jack cut Cheese in 5 lb. packages. The recall involves 363 lbs of product packed on October 4, 2016.

The recall is being conducted because a supplier recalled cheese due to the potential for contamination with Listeria monocytogenes or inadequate pasteurization. The affected product was distributed domestically in Michigan, Indiana, Illinois, Ohio, Pennsylvania, and South Dakota.

Consumers who have purchased this product should check their refrigerators for the specific 5 lb. packages of A New Dairy Pepper Jack cut Cheese packed on October 4, 2016. If found, consumers should discard the product or return it to the place of purchase.

The recalled product

Product
A New Dairy Pepper Jack cut Cheese, 5 lb. packages packed in plastic bags, keep refrigerated
Manufacturer
Kuster's Inc.

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • packed on 10/04/2016

Distribution

Distributed in 6 states:

Part of a larger recall action

This product is one of 10 recalled by Kuster's Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 10 products in this recall →

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