Wishbone Chunky Blue Cheese Dressing 24oz. bottle UPC 0-41321-00691-3; six bottles per case
Summary
The FDA issued a Class I for Wishbone Chunky Blue Cheese Dressing 24oz. bottle UPC 0-41321-00691-3; six bottl by CONAGRA BRANDS. Reason: Undeclared eggs.
Details
Source
Food Recall
External ID
F-0732-2022
Action Date
2022-02-16
Status
Terminated
Category
food
Product Description
Wishbone Chunky Blue Cheese Dressing 24oz. bottle UPC 0-41321-00691-3; six bottles per case
Lot/Code Info: Lot: 4254201320 NOV0922
Quantity Affected: 200 cases
Reason for Recall
Undeclared eggs
Distribution
Nationwide retailer distribution centers in Arkansas, Colorado, Connecticut, Iowa, Indiana, Kansas, Kentucky, Louisiana, Michigan, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Texas, and Virginia.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-01-28
Company
Chicago, IL
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 115 food recalls issued in the same week, part of 204 food-related FDA actions this month.
CONAGRA BRANDS has 3 FDA actions in our database, including 3 recalls.
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 (CONAGRA BRANDS) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does CONAGRA BRANDS have FDA actions?
CONAGRA BRANDS has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0732-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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