CLASS I Food recall · Reported 27 Jul 2022 · FDA Enforcement Report

Panera Bread at Home Southwest Corn Chowder recalled

Blount Fine Foods is recalling Panera Bread at Home Southwest Corn Chowder, distributed in 12 states. The recall was initiated on 22 Jun 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot/Unit Numbers: 042122-2K USE BY:6/30/22 UPC Codes: 077958690812
Quantity recalled15,414 units (2,569 cases)

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-1502-2022
FDA event ID
90494
Recalling firm
Blount Fine Foods, Fall River, MA
Brand
Panera
Classification
Class I
Status
Terminated
Recall initiated
22 Jun 2022
FDA classified
19 Jul 2022
Reported
27 Jul 2022
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product category
Soup

Timeline

22 Jun 2022Recall initiated by company
19 Jul 2022Classified by FDA+27 days
27 Jul 2022Published 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

Contains undeclared wheat

Product as listed by the FDA

Panera Bread at Home Southwest Corn Chowder, 16 oz. (453 g)

Where it was distributed

MA, ME, IL, IA, OH, CA, MI, NH, WA, TX, VA, NY

CaliforniaIowaIllinoisMassachusettsMaineMichiganNew HampshireNew YorkOhioTexasVirginiaWashington

Questions about this recall

Why was it recalled?

Contains undeclared wheat

Which lots are affected?

Lot/Unit Numbers: 042122-2K USE BY:6/30/22 UPC Codes: 077958690812

Where was it sold?

MA, ME, IL, IA, OH, CA, MI, NH, WA, TX, VA, NY

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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