FDA recall record
Liquid Whey; Bulk.
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
Liquid Whey; Bulk.
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.
Liquid Whey; Bulk.
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.
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: 2,220,253.9 lbs
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.