openFDAClass IITerminated

Class II: May cause temporary or reversible health effects; serious effects are unlikely

Terminated means the FDA lists this recall as closed or completed — it does not mean a product is safe.

This recall is no longer listed as ongoing. Review the status and official source below.

Market Of Choice Vegan Kale Caesar Salad recall

Source: U.S. Food and Drug Administration · Reported June 10, 2026 · Not a government service

From the FDA record

Why it was recalled

Undeclared allergen (sesame). Ingredients panel does not list sesame as sub-ingredient of Za'atar spice and Contains statement does not declare sesame.

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Market Of Choice Vegan Kale Caesar Salad
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Package size: 9.5oz · Net Wt. 9.5oz
Recall lists UPC 0210126010993
Code information
Expiration dates: 4/20/2026 4/21/2026 4/24/2026 4/25/2026 4/27/2026 4/28/2026 5/1/2026 5/2/2026 5/4/2026 5/5/2026
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Check your package against the affected product information below. The FDA enforcement record does not include product-specific return or disposal instructions. Review the official notice or contact the recalling company before taking action.

From the FDA record

Reported distribution

Only in OR state.

Distribution information reflects what was reported in the FDA record and may not include every downstream location.

Technical recall details

FDA recall number

H-0904-2026

FDA event ID

98908

Recalling firm

Market of Choice Inc

Original product description

Market of Choice Vegan Kale Caesar Salad, Net Wt. 9.5oz. Finished product is pre-packaged into a clear flexible plastic clamshell container. Label has UPC 0 210126 01099 3. Market Central Kitchen 1150 Owen Loop S. Eugene, OR 97402 The Za'atar spice, which contains Sesame Seeds, is mixed with chickpeas and packaged into a 2-oz plastic cup. This 2-oz. cup with chickpeas is then assembled into the finished product: a 9.5oz flexible clear plastic clamshell container of Vegan Kale Caesar Salad.

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Product quantity

289 (9.5oz) units

Initiation date

May 4, 2026

Report date

June 10, 2026

FDA classification

Class II

May cause temporary or reversible health effects; serious effects are unlikely

Status

Terminated

Voluntary or mandated

Voluntary: Firm initiated

Original code information

Expiration dates: 4/20/2026 4/21/2026 4/24/2026 4/25/2026 4/27/2026 4/28/2026 5/1/2026 5/2/2026 5/4/2026 5/5/2026

Products in this recall

openFDA enforcement source

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Last data refresh

2026-07-31 03:18 UTC

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