Class ITerminatedVoluntary: Firm initiated
Kradjian Importing Company, Inc.: food recall H-0576-2026
Kradjian Importing Company, Inc. of Glendale, CA recalled MID EAST Jordanian Zaatar spice mix; NET Wt. 5lb plastic bag; UPC: 094379607038 Packed by: Propack Inc. Sunvalley, CA… Reason: Undeclared allergen ingredients (sesame and wheat) in Zaatar Spice mix. The FDA listed it as Class I in its Enforcement Report dated Mar 25, 2026.
Record status as published: Terminated (terminated May 15, 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
- MID EAST Jordanian Zaatar spice mix; NET Wt. 5lb plastic bag; UPC: 094379607038 Packed by: Propack Inc. Sunvalley, CA 91354
- Product quantity
- 4,400 pounds
- Reason for recall
- Undeclared allergen ingredients (sesame and wheat) in Zaatar Spice mix.
- Codes, lots and dates on the package
- m-dd format of repacking
- Distribution pattern
- Distribution is to bakeries for further processing into various Zaatar breads and pastries.
- Recalling firm
- Kradjian Importing Company, Inc., Glendale, CA
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- 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 | Mar 6, 2026 |
| Classified by the FDA | Mar 18, 2026 |
| Published in the Enforcement Report | Mar 25, 2026 |
| Terminated | May 15, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0576-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.