RecallHawk
Class I Recall

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

Blount Fine Foods Corporation

Summary

The FDA issued a Class I for Panera Bread at Home Southwest Corn Chowder, 16 oz. (453 g) by Blount Fine Foods Corporation. Reason: Contains undeclared wheat.

Details

Source

Food Recall

External ID

F-1502-2022

Action Date

2022-07-27

Status

Terminated

Category

food

Product Description

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

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

Quantity Affected: 15,414 units (2,569 cases)

Reason for Recall

Contains undeclared wheat

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2022-06-22

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 88 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Blount Fine Foods Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Blount Fine Foods Corporation have FDA actions?

This is the only FDA action we have on record for Blount Fine Foods Corporation in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1502-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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