Dreamland's Zaatar Chickpea Salad is packaged in poly bags with a generic label which declares "chickpeas, cumin, zataar
Summary
The FDA issued a Class I for Dreamland's Zaatar Chickpea Salad is packaged in poly bags with a generic label by Dreamland Inc. Reason: Undeclared Sesame, Soy, Wheat.
Details
Source
Food Recall
External ID
H-0575-2026
Action Date
2026-03-25
Status
Terminated
Category
food
Product Description
Dreamland's Zaatar Chickpea Salad is packaged in poly bags with a generic label which declares "chickpeas, cumin, zataar, turmeric, dill, onion, garlic, parsley". Dreamland distributed bulk cases (2/5lbs. bags per case) to Haggen store. Bulk 5lbs. bags were not sold directly to consumers. Haggen stores unpacked 5lb. bags of chickpea salad into cold food pan at salad bar (without mixing with other ingredients), consumers packed product in grab & go containers, and Haggen applied scale label when members paid at the register.
Lot/Code Info: Sell by 02/28/26 Sell by 03/01/26
Quantity Affected: 30lbs.
Reason for Recall
Undeclared Sesame, Soy, Wheat
Distribution
Distributed in WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-02-25
Company
Seattle, WA
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 (Dreamland Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Dreamland Inc have FDA actions?
This is the only FDA action we have on record for Dreamland Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0575-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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