Class IITerminatedVoluntary: Firm initiated
Market of Choice Inc: food recall H-0904-2026
Market of Choice Inc of Eugene, OR recalled Market of Choice Vegan Kale Caesar Salad, Net Wt. 9.5oz. Finished product is pre-packaged into a clear flexible… Reason: Undeclared allergen (sesame). Ingredients panel does not list sesame as sub-ingredient of Za'atar spice and Contains statement does not declare sesame. The FDA listed it as Class II in its Enforcement Report dated Jun 10, 2026; distribution: Oregon.
Record status as published: Terminated (terminated Jun 8, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- 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.
- Product quantity
- 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.
- Codes, lots and dates on the package
- 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
- Distribution pattern
- Only in OR state.
- Recalling firm
- Market of Choice Inc, Eugene, OR
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 4, 2026 |
| Classified by the FDA | Jun 3, 2026 |
| Published in the Enforcement Report | Jun 10, 2026 |
| Terminated | Jun 8, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0904-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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