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Class ITerminated in FDA datasetRecall initiated Dec 21, 2018

Dakota Specialty Milling Milton's MG Premix w Enrichment 94503860, 41820, Net Wt 50 lbs. Yellow…

Recalling firm: Dakota Specialty Milling, Inc

Why it was recalled

An ingredient in the blended products has the potential to be contaminated with Salmonella.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 13, 2019.

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Compare the exact product and package details with the label you have.

ProductDakota Specialty Milling Milton's MG Premix w Enrichment 94503860, 41820, Net Wt 50 lbs. Yellow Corn, Wheat Bran, Oat Fiber, Enrichment Blend (Contains: Vitamins B1, B2, B3, B6, B12; Pantothenic Acid; Zinc; Wheat Starch), Bread Softener, (contains Wheat Flour, Enzymes), Ferrous Sulfate (contains Wheat Starch)
Package size50 lbs

FDA code information

Lot codes: 10271803, 10291803, 11081803, 11091803, 12131803, 12141803

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Dakota Specialty Milling Milton's MG Premix w Enrichment 94503860, 41820, Net Wt 50 lbs. Yellow Corn, Wheat Bran, Oat Fiber, Enrichment Blend (Contains: Vitamins B1, B2, B3, B6, B12; Pantothenic Acid; Zinc; Wheat Starch), Bread Softener, (contains Wheat Flour, Enzymes), Ferrous Sulfate (contains Wheat Starch)

Extracted codes and context

TypeCode / valueContext
lot10271803Lot codes: 10271803, 10291803, 11081803, 11091803, 12131803, 12141803
lot10291803Lot codes: 10271803, 10291803, 11081803, 11091803, 12131803, 12141803
lot11081803Lot codes: 10271803, 10291803, 11081803, 11091803, 12131803, 12141803
lot11091803Lot codes: 10271803, 10291803, 11081803, 11091803, 12131803, 12141803
lot12131803Lot codes: 10271803, 10291803, 11081803, 11091803, 12131803, 12141803
lot12141803Lot codes: 10271803, 10291803, 11081803, 11091803, 12131803, 12141803

Original FDA recall reason

An ingredient in the blended products has the potential to be contaminated with Salmonella.

Recall details

Recall number
F-0937-2019
Event ID
81907
FDA status
Terminated
Initiated
Dec 21, 2018
Reported
Feb 6, 2019
Classified
Feb 14, 2019
Terminated
May 13, 2019
Quantity
92,150 lbs.
Location
Fargo, ND, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

CA, OH, TX

FDA source record · F-0937-2019

Data updated September 16, 2026. View official FDA data ↗

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