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Class I: serious health riskTerminated

Deutsch Kase Haus Colby cheese Recall

Colby cheese

Deutsch Kase Haus, LLC · Middlebury, IN

Risk level
Class I
Reported by FDA
May 3, 2017
Recall ID
F-1887-2017
Check your lot numberHow we source this data

Summary

Deutsch Kase Haus recalled Colby cheese starting Feb 5, 2017. The FDA classified it as Class I (serious health risk) and published enforcement report F-1887-2017 on May 3, 2017. Reason: Potential Listeria monocytogenes contamination. Status: Terminated.

Why it was recalled

Potential Listeria monocytogenes contamination.

Product description

Colby cheese. All affected product private labeled for other companies. Brands: Guggisberg; Dutch Farms; Meijer; Amish Classics; Lipari Old Tyme; Laubscher; Walnut Creek; Copperwood; Dietz & Watson; Banquet; 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 39 slicer 4 diameter x 39 long cylinder (single per case) Products package in clear plastic bags. Bags sealed by vacuum sealing and shrink wrapping.

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. 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: W0105; L0104-85; L0102-86; L0102-71; L0102-70; L0102-65; L0102-64; L0102-63; D0102-86; D0102-83; D0102-82; D0102-72; D0102-71; D0102-70; D0102-65; D0102-64; S0101

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-1887-2017
Classification
Class I
Status
Terminated
Recall initiated
Feb 5, 2017
FDA report date
May 3, 2017
Quantity
4,121,370.18 lbs (total cheese/cheese products)
Recall type
Voluntary: Firm initiated
Recalling firm
Deutsch Kase Haus, LLC

Original FDA data

Every field from FDA enforcement report F-1887-2017, 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. 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: W0105; L0104-85; L0102-86; L0102-71; L0102-70; L0102-65; L0102-64; L0102-63; D0102-86; D0102-83; D0102-82; D0102-72; D0102-71; D0102-70; D0102-65; D0102-64; S0101
Postal code
46540-7708
Report date
May 3, 2017
Product type
Food
Recall number
F-1887-2017
Classification
Class I
Recalling firm
Deutsch Kase Haus, LLC
Product quantity
4,121,370.18 lbs (total cheese/cheese products)
Termination date
Oct 5, 2017
Reason for recall
Potential Listeria monocytogenes contamination.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Colby cheese. All affected product private labeled for other companies. Brands: Guggisberg; Dutch Farms; Meijer; Amish Classics; Lipari Old Tyme; Laubscher; Walnut Creek; Copperwood; Dietz & Watson; Banquet; 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 39 slicer 4 diameter x 39 long cylinder (single per case) Products package in clear plastic bags. Bags sealed by vacuum sealing and shrink wrapping.
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-1887-2017, published May 3, 2017. View the source record (openFDA) · FDA enforcement reports

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

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