FDA recall record
Pepper Colby-Jack (or: Pepper Marble Jack; Lightning Jack; Thunder Jack; Firecracker; Jalapeno Jack; Jumping Jack) cheese. All affected product private labeled for other compan...
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of October 5, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Pepper Colby-Jack (or: Pepper Marble Jack; Lightning Jack; Thunder Jack; Firecracker; Jalapeno Jack; Jumping Jack) cheese. All affected product private labeled for other companies.
Brands: Guggisberg; Dutch Farms; Amish Classics; Lipari Old Tyme; Walnut Creek; Product packaged as: 6lb deli horns (4 diameter x 13 long cylinder) 2 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 shrink wrapping.
Reason
Potential Listeria monocytogenes contamination.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Pepper Colby-Jack (or: Pepper Marble Jack; Lightning Jack; Thunder Jack; Firecracker; Jalapeno Jack; Jumping Jack) cheese. All affected product private labeled for other companies.
Brands: Guggisberg; Dutch Farms; Amish Classics; Lipari Old Tyme; Walnut Creek; Product packaged as: 6lb deli horns (4 diameter x 13 long cylinder) 2 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 shrink wrapping.
Code information listed by FDA
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: D0602-83; D0602-71; D0602-70; D0602-65; D0602-64; W0605
Distribution and firm information
Recalling firm listed by FDA: Deutsch Kase Haus, LLC
Firm location listed by FDA: Middlebury, IN, United States
Distribution reported by FDA: IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN, and IN
Product quantity listed by FDA: 4,121,370.18 lbs (total cheese/cheese products)
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.