Kradjian Importing Company, Inc. food recall: MID EAST Jordanian Zaatar spice mix
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 98559
- Recall initiated
- Mar 6, 2026
- Classified by FDA
- Mar 18, 2026
- Posted in Enforcement Report
- Mar 25, 2026
- Terminated
- May 15, 2026
- Recalling firm
- Kradjian Importing Company, Inc.
- Firm location
- Glendale, CA, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Undeclared allergen ingredients (sesame and wheat) in Zaatar Spice mix.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Mar 6, 2026. FDA classified it 12 days later, on Mar 18, 2026. Distribution reported by FDA: Distribution is to bakeries for further processing into various Zaatar breads and pastries. Kradjian Importing Company, Inc. has 2 recalls in our records.
Recalled products (1)
H-0576-2026 Class I Terminated
MID EAST Jordanian Zaatar spice mix; NET Wt. 5lb plastic bag; UPC: 094379607038 Packed by: Propack Inc. Sunvalley, CA 91354
Codes / lots: m-dd format of repacking
Quantity: 4,400 pounds
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 98559
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.