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Class II: temporary or reversible health riskTerminated

Ardent Mills Safeguard Soft Flr Recall

Safeguard Soft Flr (GIV) packaged in 50 lb bags

Ardent Mills, LLC · Omaha, NE

Risk level
Class II
Reported by FDA
Oct 24, 2018
Recall ID
F-0030-2019
Check your lot numberHow we source this data

Summary

Ardent Mills recalled Safeguard Soft Flr starting Sep 13, 2018. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0030-2019 on Oct 24, 2018. Reason: Flour tested positive for Salmonella by customer. Status: Terminated.

Why it was recalled

Flour tested positive for Salmonella by customer.

Product description

Safeguard Soft Flr (GIV) packaged in 50 lb bags

Lot numbers, UPCs & expiration codes

423810

Where it was sold

Distributor to manufacturer in Illinois

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-0030-2019
Classification
Class II
Status
Terminated
Recall initiated
Sep 13, 2018
FDA report date
Oct 24, 2018
Quantity
7,500 lbs
Recall type
Voluntary: Firm initiated
Recalling firm
Ardent Mills, LLC

Original FDA data

Every field from FDA enforcement report F-0030-2019, exactly as published.

Show all FDA fields
City
Omaha
State
NE
Status
Terminated
Country
United States
Event ID
81035
Address
2900 C St
Code information
423810
Postal code
68107-1589
Report date
Oct 24, 2018
Product type
Food
Recall number
F-0030-2019
Classification
Class II
Recalling firm
Ardent Mills, LLC
Product quantity
7,500 lbs
Termination date
Oct 23, 2018
Reason for recall
Flour tested positive for Salmonella by customer.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Safeguard Soft Flr (GIV) packaged in 50 lb bags
Distribution pattern
Distributor to manufacturer in Illinois
Recall initiation date
Sep 13, 2018
Initial firm notification
Visit
Center classification date
Oct 15, 2018

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0030-2019, published Oct 24, 2018. View the source record (openFDA) · FDA enforcement reports

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

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