CLASS I Food recall · Reported 27 Sep 2017 · FDA Enforcement Report

Cabernet Grille Butter recalled by Dierbergs Markets, Inc

Dierbergs Markets, Inc Corporate Office is recalling Cabernet Grille Butter, distributed in Illinois, Missouri. The recall was initiated on 14 Aug 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesSell-by dates 11/3/17 and earlier.
Quantity recalled709 3 oz packages

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-3559-2017
FDA event ID
77946
Recalling firm
Dierbergs Markets, Inc Corporate Office, Chesterfield, MO
Classification
Class I
Status
Terminated
Recall initiated
14 Aug 2017
FDA classified
19 Sep 2017
Reported
27 Sep 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product category
Butter

Timeline

14 Aug 2017Recall initiated by company
19 Sep 2017Classified by FDA+36 days
27 Sep 2017Published in enforcement report+8 days

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

Reason for recall

Flavored butter contains undeclared wheat and soy.

Product as listed by the FDA

Cabernet Grille Butter, Net Wt. 3 OZ, packaged in clear plastic tubs. Dierbergs Kitchens

Where it was distributed

Distributed to retail grocery stores in central and western Missouri and eastern Illinois.

IllinoisMissouri

Questions about this recall

Is Cabernet Grille Butter recalled?

Yes. Dierbergs Markets, Inc Corporate Office recalled Cabernet Grille Butter on 14 Aug 2017. The recall is Class I and its status is Terminated. Recall number F-3559-2017.

Why was it recalled?

Flavored butter contains undeclared wheat and soy.

Which lots are affected?

Sell-by dates 11/3/17 and earlier.

Where was it sold?

Distributed to retail grocery stores in central and western Missouri and eastern 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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 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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