CLASS II Food recall · Reported 24 Oct 2018 · FDA Enforcement Report

Safeguard Soft Flr (GIV) recalled by Ardent Mills

Ardent Mills is recalling Safeguard Soft Flr (GIV), distributed in Illinois. The recall was initiated on 13 Sep 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes423810
Quantity recalled7,500 lbs

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0030-2019
FDA event ID
81035
Recalling firm
Ardent Mills, Omaha, NE
Classification
Class II
Status
Terminated
Recall initiated
13 Sep 2018
FDA classified
15 Oct 2018
Reported
24 Oct 2018
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Salmonella
Product category
Other

Timeline

13 Sep 2018Recall initiated by company
15 Oct 2018Classified by FDA+32 days
24 Oct 2018Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Flour tested positive for Salmonella by customer.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Safeguard Soft Flr (GIV) packaged in 50 lb bags

Where it was distributed

Distributor to manufacturer in Illinois

Illinois

Questions about this recall

Why was it recalled?

Flour tested positive for Salmonella by customer.

Which lots are affected?

423810

Where was it sold?

Distributor to manufacturer in Illinois

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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