CLASS II Food recall · Reported 26 Jun 2024 · FDA Enforcement Report

Tuscan Salad Bowl Ingredients recalled by Heinens

Heinens is recalling Tuscan Salad Bowl Ingredients: Garbanzo Beans***Disodium EDTA***Arugula, Roasted, distributed in Illinois, Ohio. The recall was initiated on 30 May 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesMR252818
Quantity recalled106 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-1377-2024
FDA event ID
94751
Recalling firm
Heinens, Warrensville Heights, OH
Classification
Class II
Status
Terminated
Recall initiated
30 May 2024
FDA classified
18 Jun 2024
Reported
26 Jun 2024
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Tree Nuts
Product category
Salad Kits

Timeline

30 May 2024Recall initiated by company
18 Jun 2024Classified by FDA+19 days
26 Jun 2024Published 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

Product contains undeclared pecans, a known allergen.

Product as listed by the FDA

Heinen's Tuscan Salad Bowl Ingredients: Garbanzo Beans***Disodium EDTA***Arugula, Roasted Corn***Red Bell Pepper, Dried Cranberries***Walnuts***Parmesan Cheese*** Contains: WALNUT, MILK

Where it was distributed

Product was only distributed to Heinen retail locations in Illinois and Ohio.

IllinoisOhio

Questions about this recall

Why was it recalled?

Product contains undeclared pecans, a known allergen.

Which lots are affected?

MR252818

Where was it sold?

Product was only distributed to Heinen retail locations in Illinois and Ohio.

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 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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