Skip to main content
High RiskFDAfda-F-0742-2016UNDECLARED ALLERGEN

Urban Oven Artisan-Baked Short Bread Cookies Classic Butter All Natural NET WT. 5 oz. UPC Code: 7 18122 06344 4 SKU #: C1000

Category
Units Affected
757
Recall Date
February 9, 2016
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0742-2016.

Urban Oven, LLC is recalling Urban Oven Butter Cookies, Cocoa Cookies, Pecan Cookies, and Lemon Pistachio Cookies because it does not declare milk on the label from the ingredient butter.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0742-2016.

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 Urban Oven, 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-0742-2016.

Urban Oven, 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

Urban Oven, Llc Recall FAQ

Urban Oven, Llc is the subject of a dairy safety report: Urban Oven Artisan-Baked Short Bread Cookies Classic Butter All Natural NET WT. 5 oz. UPC Code: 7 18122 06344 4 SKU #: C1000. The notice was published on February 9, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 757 units are potentially affected.