Recalls / Class I
Class IF-1898-2017
Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.
Product
Liquid Whey; Bulk.
- Type
- Food
- Affected lot / code info
- All lots in market manufactured from 9/1/2016 to 1/27/2017 and distributed from 9/1/2016 to 2/7/2017.
- Quantity
- 2,220,253.9 lbs
Why it was recalled
Potential Listeria monocytogenes contamination.
Recalling firm
- Firm
- Deutsch Kase Haus, LLC
- Notification channel
- Type
- Voluntary: Firm initiated
- Address
- 11275 W 250 N, N/A, Middlebury, Indiana 46540-7708
Distribution
- Distribution pattern
- IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN, and IN
Timeline
- Recall initiated
- 2017-02-05
- FDA classified
- 2017-04-24
- Posted by FDA
- 2017-05-03
- Terminated
- 2017-10-05
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-1898-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings.