MID EAST Jordanian Zaatar spice mix; NET Wt. 5lb plastic bag; UPC: 094379607038 Packed by: Propack Inc. Sunvalley, CA
Summary
The FDA issued a Class I for MID EAST Jordanian Zaatar spice mix; NET Wt. 5lb plastic bag; UPC: 094379607038 by Kradjian Importing Company, Inc.. Reason: Undeclared allergen ingredients (sesame and wheat) in Zaatar Spice mix..
Details
Source
Food Recall
External ID
H-0576-2026
Action Date
2026-03-25
Status
Terminated
Category
food
Product Description
MID EAST Jordanian Zaatar spice mix; NET Wt. 5lb plastic bag; UPC: 094379607038 Packed by: Propack Inc. Sunvalley, CA 91354
Lot/Code Info: m-dd format of repacking
Quantity Affected: 4,400 pounds
Reason for Recall
Undeclared allergen ingredients (sesame and wheat) in Zaatar Spice mix.
Distribution
Distribution is to bakeries for further processing into various Zaatar breads and pastries.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-03-06
Company
Glendale, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 48 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Kradjian Importing Company, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Kradjian Importing Company, Inc. have FDA actions?
This is the only FDA action we have on record for Kradjian Importing Company, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0576-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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