Dreamland's Zaatar Chickpea Salad is packaged in poly bags with a… recall
Recalled by Dreamland Inc · Seattle, WA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Undeclared Sesame, Soy, Wheat
Undeclared allergens: Soy Wheat Sesame
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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.
Quantity: 30lbs.
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Sell by 02/28/26 Sell by 03/01/26
Where it was sold
Washington
FDA's distribution note: Distributed in WA.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to soy, wheat, sesame; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Dreamland Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 25, 2026
- In FDA report of
- Mar 25, 2026
- Terminated
- Mar 24, 2026
- FDA recall number
- H-0575-2026 · event 98499
- Official record
- FDA enforcement report search