Skip to main content
RecallFDAfda-F-1790-2022UNDECLARED ALLERGEN

Alida's Samoon Pita Bread, 4 pieces per package, net wt. 21 oz. UPC 8 60004 65933 4. Product contains ingredients: While Flour, Water, ...

Units Affected
19
Recall Date
August 16, 2022
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1790-2022.

Undeclared soy lecithin. The canola oil used to grease pans was found to contain soy lecithin.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1790-2022.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Alida's Bakery Llc or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1790-2022.

Alida's Bakery LLC

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Alida's Bakery Llc Recall FAQ

Alida's Bakery Llc is the subject of a bakery & grains safety report: Alida's Samoon Pita Bread, 4 pieces per package, net wt. 21 oz. UPC 8 60004 65933 4. Product contains ingredients: While Flour, Water, .... The notice was published on August 16, 2022 by the U.S. Food and Drug Administration (FDA). Approximately 19 units are potentially affected.