The Recall Desk
Agency classClass IOur severity:CriticalFDA (Food)·F-1899-2017·Announced 2017-05-03

Deutsch Kase Haus Recalls Bulk Cream for Listeria Risk

Deutsch Kase Haus, LLC is recalling bulk cream due to potential Listeria monocytogenes contamination. The product was distributed to multiple states.

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 5/5 (Critical).

Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The FDA has classified this as a Class I recall, which meets the rubric criteria for a Critical severity score.

Plain-English summary

Deutsch Kase Haus, LLC is recalling 86,612.7 lbs of bulk cream due to potential Listeria monocytogenes contamination. The recall covers all lots in market manufactured from September 1, 2016, to January 27, 2017, and distributed from September 1, 2016, to February 7, 2017.

The affected product was distributed in Illinois, Ohio, Wisconsin, Nevada, Alabama, Arizona, Pennsylvania, Tennessee, Michigan, Minnesota, and Indiana. The U.S. Food and Drug Administration has classified this as a Class I recall, which is the most serious type of recall.

Consumers who have purchased this product should stop using it and contact the manufacturer or their local health department for further instructions.

The recalled product

Product
Cream; Bulk.
Hazard

Distribution

Distributed in 11 states:

Part of a larger recall action

This product is one of 13 recalled by Deutsch Kase Haus, LLC 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 13 products in this recall →

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