Cranberry Orange Scone, brand Mad Batter Bakery, net wt. 5 oz per unit. Product is sold in a plastic film wrapper with labeling on the b...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1085-2017.
Cranberry Orange Scones are recalled because they may contain undeclared Milk, Egg, Soy, and Wheat.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1085-2017.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Thomas Hammer Coffee Roasters, Inc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- 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-1085-2017.
Thomas Hammer Coffee Roasters, Inc.
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.
Thomas Hammer Coffee Roasters, Inc. Recall FAQ
Thomas Hammer Coffee Roasters, Inc. is the subject of a produce safety report: Cranberry Orange Scone, brand Mad Batter Bakery, net wt. 5 oz per unit. Product is sold in a plastic film wrapper with labeling on the b.... The notice was published on December 14, 2016 by the U.S. Food and Drug Administration (FDA). Approximately 52 units are potentially affected.