Market of Choice Vegan Kale Caesar Salad, Net Wt. 9.5oz. Finished product is pre-packaged into a clear flexible plastic
Summary
The FDA issued a Class II for Market of Choice Vegan Kale Caesar Salad, Net Wt. 9.5oz. Finished product is pre by Market of Choice Inc. Reason: Undeclared allergen (sesame). Ingredients panel does not list sesame as sub-ingredient of Za'atar spice and Contains statement does not declare sesame.
Details
Source
Food Recall
External ID
H-0904-2026
Action Date
2026-06-10
Status
Terminated
Category
food
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.
Lot/Code Info: 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
Quantity Affected: 289 (9.5oz) units
Reason for Recall
Undeclared allergen (sesame). Ingredients panel does not list sesame as sub-ingredient of Za'atar spice and Contains statement does not declare sesame.
Distribution
Only in OR state.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-04
Company
Eugene, OR
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 166 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (Market of Choice Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Market of Choice Inc have FDA actions?
This is the only FDA action we have on record for Market of Choice Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0904-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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