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Class I: serious health riskTerminated

Deutsch Kase Haus Cream Recall

Cream; Bulk.

Deutsch Kase Haus, LLC · Middlebury, IN

Risk level
Class I
Reported by FDA
May 3, 2017
Recall ID
F-1899-2017
Check your lot numberHow we source this data

Summary

Deutsch Kase Haus recalled Cream starting Feb 5, 2017. The FDA classified it as Class I (serious health risk) and published enforcement report F-1899-2017 on May 3, 2017. Reason: Potential Listeria monocytogenes contamination. Status: Terminated.

Why it was recalled

Potential Listeria monocytogenes contamination.

Product description

Cream; Bulk.

Lot numbers, UPCs & expiration codes

All lots in market manufactured from 9/1/2016 to 1/27/2017 and distributed from 9/1/2016 to 2/7/2017.

Where it was sold

IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN, and IN

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1899-2017
Classification
Class I
Status
Terminated
Recall initiated
Feb 5, 2017
FDA report date
May 3, 2017
Quantity
86,612.7 lbs
Recall type
Voluntary: Firm initiated
Recalling firm
Deutsch Kase Haus, LLC

Original FDA data

Every field from FDA enforcement report F-1899-2017, exactly as published.

Show all FDA fields
City
Middlebury
State
IN
Status
Terminated
Country
United States
Event ID
76426
Address
11275 W 250 N
Code information
All lots in market manufactured from 9/1/2016 to 1/27/2017 and distributed from 9/1/2016 to 2/7/2017.
Postal code
46540-7708
Report date
May 3, 2017
Product type
Food
Recall number
F-1899-2017
Classification
Class I
Recalling firm
Deutsch Kase Haus, LLC
Product quantity
86,612.7 lbs
Termination date
Oct 5, 2017
Reason for recall
Potential Listeria monocytogenes contamination.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Cream; Bulk.
Distribution pattern
IL, OH, WI, NV, AL, AZ, PA, TN, MI, MN, and IN
Recall initiation date
Feb 5, 2017
Initial firm notification
E-Mail
Center classification date
Apr 24, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1899-2017, published May 3, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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