CLASS II Food recall · Reported 18 Mar 2020 · FDA Enforcement Report

Chicken Cobb Salad recalled by Meijer

Meijer is recalling Meijer Chicken Cobb Salad, distributed in Illinois, Indiana, Kentucky, Michigan, Ohio, Wisconsin. The recall was initiated on 25 Feb 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSell By: Mar 02, 2020
Quantity recalled360 units

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-0824-2020
FDA event ID
85095
Recalling firm
Meijer, Grand Rapids, MI
Brand
Meijer
Classification
Class II
Status
Terminated
Recall initiated
25 Feb 2020
FDA classified
10 Mar 2020
Reported
18 Mar 2020
Type
Voluntary: Firm initiated
Customers notified by
Other
Product category
Salad Kits

Timeline

25 Feb 2020Recall initiated by company
10 Mar 2020Classified by FDA+14 days
18 Mar 2020Published 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

Undeclared wheat allergen, salad may incorrectly contain a packet of croutons.

Product as listed by the FDA

Meijer Chicken Cobb Salad 10.75oz. in Clear plastic, sectioned, container; UPC 71928367932

Where it was distributed

Meijer stores in MI, OH, IN, IL, WI and KY

IllinoisIndianaKentuckyMichiganOhioWisconsin

Stores named: Meijer

Questions about this recall

Is Chicken Cobb Salad recalled?

Yes. Meijer recalled Chicken Cobb Salad on 25 Feb 2020. The recall is Class II and its status is Terminated. Recall number F-0824-2020.

Why was it recalled?

Undeclared wheat allergen, salad may incorrectly contain a packet of croutons.

Which lots are affected?

Sell By: Mar 02, 2020

Where was it sold?

Meijer stores in MI, OH, IN, IL, WI and KY

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 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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