CLASS I Food recall · Reported 4 Mar 2020 · FDA Enforcement Report

chef's recipe Mushroom Barley Soup recalled by Bakkavor Foods USA

Bakkavor Foods USA is recalling chef's recipe Mushroom Barley Soup, distributed in North Carolina. The recall was initiated on 29 Jan 2020 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesSELL BY 03/09/20 Lot 975002
Quantity recalled840/16 OZ containers

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-0798-2020
FDA event ID
84830
Recalling firm
Bakkavor Foods USA, Charlotte, NC
Classification
Class I
Status
Terminated
Recall initiated
29 Jan 2020
FDA classified
6 Mar 2020
Reported
4 Mar 2020
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Milk
Product category
Soup

Timeline

29 Jan 2020Recall initiated by company
4 Mar 2020Published in enforcement report+35 days
6 Mar 2020Classified by FDA+2 days

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

Reason for recall

The product contains undeclared milk.

Product as listed by the FDA

chef's recipe MUSHROOM BARLEY SOUP NET WT 16 OZ (1LB) 454g PROUDLY DISTRIBUTED BY: HARRIS TEETER, LLC, MATTHEWS, NC 28105 UPC 1 61088 80363 0

Where it was distributed

Product was distributed to distribution centers in NC

North Carolina

Stores named: Kroger

Questions about this recall

Why was it recalled?

The product contains undeclared milk.

Which lots are affected?

SELL BY 03/09/20 Lot 975002

Where was it sold?

Product was distributed to distribution centers in NC

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 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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