RecallHawk
Class I Recall

Fresh From Meijer Chicken Caesar Salad 6.4 Oz UPC - 760236117452 Fresh From Meijer Chicken Caesar Shareable Salad 10 Oz

Meijer Inc

Summary

The FDA issued a Class I for Fresh From Meijer Chicken Caesar Salad 6.4 Oz UPC - 760236117452 Fresh From Meij by Meijer Inc. Reason: Listeria monocytogenes.

Details

Source

Food Recall

External ID

F-0831-2023

Action Date

2023-05-17

Status

Terminated

Category

food

Product Description

Fresh From Meijer Chicken Caesar Salad 6.4 Oz UPC - 760236117452 Fresh From Meijer Chicken Caesar Shareable Salad 10 Oz UPC - 719283679338

Lot/Code Info: Sell by 3/19/2023 to 3/28/2023

Quantity Affected: 9764

Reason for Recall

Listeria monocytogenes

Distribution

Meijer stores in Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin

Type: Voluntary: Firm initiated

Recall Initiated: 2023-04-05

Company

Meijer Inc

Grand Rapids, MI

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 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Meijer Inc has 18 FDA actions in our database, including 18 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 (Meijer Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Meijer Inc have FDA actions?

Meijer Inc has 18 FDA actions in our database, including 18 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0831-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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