Skip to main content
High RiskFDAfda-F-0346-2018OTHER

Arise Gluten Free Bakery Dark and Seedy Sourdough; NET WEIGHT 24 OZ (680 grams) UPC 0952256000067 Tony s item # 12485

Category
Units Affected
25
Recall Date
November 13, 2017
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0346-2018.

Firm received a complaint from a customer reporting that small shards of glass were found on the top of a slice of bread.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0346-2018.

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 Arise Gluten Free Bakery 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-0346-2018.

Arise Gluten Free Bakery

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

Arise Gluten Free Bakery Recall FAQ

Arise Gluten Free Bakery is the subject of a food safety report: Arise Gluten Free Bakery Dark and Seedy Sourdough; NET WEIGHT 24 OZ (680 grams) UPC 0952256000067 Tony s item # 12485. The notice was published on November 13, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 25 units are potentially affected.