Pepper-Jack Cheese (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
Pepper-Jack cheese. All affected product private labeled for other companies. Brands: Guggisberg; Dutch Farms; Amish Classics; Lipari Old Tyme; Laubscher; Walnut Creek; Copperwood; Product packaged as: 6lb deli horns (4 diameter x 13 long cylinder) 2 or 4 per case; 15lb long horns (6 diameter x 13 long cylinder) 2 or 4 per case; 1lb Cut and Wrap ( 4 or 6 diameter x 1 thick pucks) 10 per case Products package in clear plastic bags. Bags sealed by vacuum sealing and shrin
Brand
Deutsch Kase Haus, LLC
Lot Codes / Batch Numbers
12/2/16, vat 7 = lot# 12/2/16 V7) Item #'s: L0502-86, L0502-70, D0504-63, D0502-86, D0502-83, D0502-65, D0502-71, D0502-70, D0502-64, W0505
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. Lot numbers are printed on bag and case label. Lot# is the manufacturing date plus vat number (example: manufacturing date, 12/2/16; vat 7 = lot# 12/2/16 V7) Item #'s: L0502-86; L0502-70; D0504-63; D0502-86; D0502-83; D0502-65; D0502-71; D0502-70; D0502-64; W0505
Deutsch Kase Haus, LLC is recalling Pepper-Jack cheese. All affected product private labeled for other companies. Brands: Guggisbe 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