CLASS II Food recall · Reported 5 Feb 2020 · FDA Enforcement Report

Essential Everyday, Unbleached Flour recalled by UNFI General Corporate

Unfi General Corporate is recalling Essential Everyday, Unbleached Flour, Enriched All-Purpose Pre-Sifted. The recall was initiated on 13 Dec 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot code 481123- Best by date 12/07/2020
Quantity recalled1440 bags

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-0561-2020
FDA event ID
84552
Recalling firm
Unfi General Corporate, Providence, RI
Classification
Class II
Status
Terminated
Recall initiated
13 Dec 2019
FDA classified
24 Jan 2020
Reported
5 Feb 2020
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Salmonella
Product category
Flour

Timeline

13 Dec 2019Recall initiated by company
24 Jan 2020Classified by FDA+42 days
5 Feb 2020Published in enforcement report+12 days

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

Reason for recall

Product was found positive for Salmonella

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

Essential Everyday, Unbleached Flour, Enriched All-Purpose Pre-Sifted, packaged in a 5lb paper bag

Where it was distributed

The firm distributed this product to one consignee

Questions about this recall

Why was it recalled?

Product was found positive for Salmonella

Which lots are affected?

Lot code 481123- Best by date 12/07/2020

Where was it sold?

The firm distributed this product to one consignee

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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