FDA recall record

MDS Foods Cheddar Cheese packaged as recall — FDA F-1702-2017

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

Class Iclassification
F-1702-2017official record ID
Mar 29, 2017report date

Recall record at a glance

Official recordF-1702-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmMDS Foods Inc.
Report dateMar 29, 2017
Recall initiation dateFeb 4, 2017
Quantity37462.8 lbs
LocationMassillion, OH, United States

Official product description

Cheddar Cheese packaged as: (a) AMISH CLASSICS Cheddar Mild Color, Item 28311, 10 lbs, No UPC (b) Deli Made EZ Cheddar Mild Stick, Item 28532, 4.5 lbs, no UPC (c) Deli Made EZ Cheddar Mild C St Pk .75oz Slice, Item 28545, 2 lbs, UPC 828653285458 (d) AMISH CLASSICS Deli Made EZ Cheddar St Pk .75oz Slice, Item 28553, 1.5 Lbs, no UPC (e) AMISH CLASSICS Deli Made EZ Cheddar Mild Stk Pk .5oz Slice, Item 28555, 1.54 lbs, UPC 828653285557 (f) Deli Readi Cheddar St Pk 1oz Slice, Item 28831, 2 lbs, UPC 634660628771 (g) Duck Deli Cheddar Mild Color Loaf, Item 28745, 5 lbs, no UPC (h) Duck Deli Cheddar st pk .75oz Slice, Item 28747, 1.5 lbs, UPC 828653287476 (i) Madison Valley Farms Cheddar St Pk .75oz Slice, Item 28769, 1.5 lbs, UPC 828653287698 (j) Sutters Quality Foods Cheddar St Pk .75oz Slice, Item 28812, 1.5 lbs, UPC 828653288126 (k) Sutters Quality Foods Cheddar Mild Color Loaf, Item 28815, 5 lbs, no UPC (l) Troyer Cheddar EW Full Moon, Item 28841, 8 oz, UPC 49646936076

Why the product was recalled

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

Distribution information

FL, GA, IL, IN, KS, KY, MA, MI, MO, MC, OH, PA, SC, TN, TX, UT

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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