This recall is archived. It was completed or terminated more than 90 days ago.
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Dreamland Zaatar Chickpea Salad
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FOOD RECALLCRITICAL

Dreamland Zaatar Chickpea Salad

Dreamland is recalling Zaatar Chickpea Salad due to undeclared sesame, soy, and wheat allergens.

What to do

Consumers who have an allergy or severe sensitivity to sesame, soy, or wheat should not consume this product and should return it to the place of purchase for a full refund.

Recalled
Listed
Updated
Recall No.
H-0575-2026
Agency
FDA
Firm
Dreamland Inc
Recall ID
98499
Status
TERMINATED

Recall at a glance

Quantity recalled
30lbs.

Why it was recalled

This recall covers multiple undeclared allergens: soy, wheat, and sesame.

Is mine affected?

This recall covers the products below. If you have any of them, yours is affected.

Product
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
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.

Where it was sold

Distributed in Washington.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Recall ended
  4. Listed on Recall Canary
  5. Archived
  6. Summary updated
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Editorial summary by Recall Canary · summary updated 2026-07-01 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification