Skip to main content

Ended FDAEvent 98908 (5 months ago)

Market of Choice Vegan Kale Caesar Salad

Market of Choice Vegan Kale Caesar Salad contains undeclared sesame, which can cause serious allergic reactions.

Recall ended Jun 8, 2026. Still check yours.

Moderate risk

Eating it may cause temporary or medically reversible health problems. Serious harm is unlikely.

FDA Class II recall · How risk is rated

2 photos

What to do

What happened

Market of Choice Inc, of Eugene, Oregon, recalled Market of Choice Vegan Kale Caesar Salad, Net Wt. 9.5oz, on May 4, 2026, because the Za'atar spice contains sesame seeds but the ingredients panel does not list sesame as a sub-ingredient and the Contains statement does not declare it.

People with an allergy or severe sensitivity to sesame risk a serious or life-threatening allergic reaction if they consume the product. The recall was announced on May 5, 2026, and added to the FDA's Enforcement Report on June 3, 2026.

The product is pre-packaged in a clear flexible plastic clamshell container and was distributed only in Oregon. The Za'atar spice is mixed with chickpeas in a 2-oz plastic cup, which is then assembled into the 9.5oz salad. The recall covers 289 units. The company began the recall on May 4, 2026.

Summary by Recall Canary from the FDA notice.

What to do

If a code on your package matches:

  1. You may return it to your local Market of Choice for a full refund or dispose of it safely.
  2. You can contact Food Safety & Quality Assurance at 503-501-6746 or send email to ktrimp@marketofchoice.com, Monday-Friday, 8am PT-4pm PT.
  3. If you have purchased affected MOC Vegan Kale Caesar Salad and have an allergy or severe sensitivity to sesame, please do not consume it.

Is yours affected?

Affected if its UPC matches.

  1. Market of Choice Vegan Kale Caesar Salad

    UPC
    • 0 210126 01099 3

Details

Company began the recall
Event ID
98908
Recall No.
H-0904-2026
Company
Market of Choice IncEugene, Oregon
Quantity recalled
289 (9.5oz) units
Recall type
Voluntary: Firm initiated
Customers told by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
  1. Company began the recall

  2. Announced by the company

  3. Listed on Recall Canary

  4. Added to FDA's Enforcement Report · Classified by FDA

  5. Recall ended

  6. In FDA's weekly enforcement report

  7. Archived

  8. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 12, 2026 · primary source: U.S. Food and Drug Administration