Food recall
Ardent Mills, LLC recall: Safeguard Soft Flr (GIV) packaged in 50 lb bags
Ardent Mills, LLC, of Omaha, NE, recalled Safeguard Soft Flr (GIV) packaged in 50 lb bags. The FDA's reason: “Flour tested positive for Salmonella by customer.” The FDA classified it Class II: it could cause temporary or minor harm. The company began the recall voluntarily on September 13, 2018, and the FDA first listed it in its Enforcement Report of October 24, 2018. The FDA has closed the recall: it found the company did all it reasonably could to remove or correct the product.
How serious
Class II
It could cause temporary or minor harm
Why
Salmonella
Status
Terminated
Closed October 23, 2018
The recall
- Company
- Ardent Mills, LLC (Omaha, NE)
- Reason, in FDA's words
- “Flour tested positive for Salmonella by customer.”
- Where it was sold
- Distributor to manufacturer in Illinois
- Recall began
- , by the company
- FDA classified it
- First in an FDA Enforcement Report
- FDA event number
- 81035
The product recalled
As the FDA describes them, with the codes that tell whether a package is part of the recall.
-
F-0030-2019 Class II
Safeguard Soft Flr (GIV) packaged in 50 lb bags
Codes: 423810
Quantity: 7,500 lbs
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Source and notes
U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of October 24, 2018.
Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.