Cheese By-Products (Deutsch Kase Haus) – Listeria Risk (2017)
Class I: 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
Class I recall indicates potential for serious health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Cheese by-products. Fines small particles of cheese curds off of the whey. Pressed Horns end of day cheese left over that is not enough to press in a tower or deli press gets pressed using the traditional press and sold as pressed horns. Split Horns co-mingled cheese portion produced in tower when changing from processing one cheese variety to another. #2 during processing if cheese does not meet specification (too dry, not enough salt). Trims ends that are removed from horns before
Brand
Deutsch Kase Haus, LLC
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
All lots in market manufactured from 9/1/2016 to 1/27/2017 and distributed from 9/1/2016 to 2/7/2017.
Deutsch Kase Haus, LLC is recalling Cheese by-products. Fines small particles of cheese curds off of the whey. Pressed Horns end o due to Potential Listeria monocytogenes contamination.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential Listeria monocytogenes contamination.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, IL, IN, MI, MN, NV, OH, PA, TN, WI
Page updated: Jan 6, 2026