Thomas Hammer Coffee Roasters Cranberry Orange Scone Recall

Why it was recalled

Cranberry Orange Scones are recalled because they may contain undeclared Milk, Egg, Soy, and Wheat.

Product description

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 back of the package.

Lot numbers, UPCs & expiration codes

no codes

Where it was sold

distributed in WA

What to do if you have this product

Compare the brand, size, and lot/UPC codes on your package with the codes above.
If it matches, don't eat it. Return it to the store for a refund or throw it away.
Wash surfaces and containers that touched the product.
If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number: F-1085-2017
Classification: Class I
Status: Terminated
Recall initiated: Dec 14, 2016
FDA report date: Jan 4, 2017
Quantity: 52/ 5 oz. units
Recall type: Voluntary: Firm initiated
Recalling firm: Thomas Hammer Coffee Roasters, Inc.

Original FDA data

Every field from FDA enforcement report F-1085-2017, exactly as published.

Show all FDA fields

City: Spokane
State: WA
Status: Terminated
Country: United States
Event ID: 75959
Address: 210 W Pacific Ave
Code information: no codes
Postal code: 99201-3624
Report date: Jan 4, 2017
Product type: Food
Recall number: F-1085-2017
Classification: Class I
Recalling firm: Thomas Hammer Coffee Roasters, Inc.
Product quantity: 52/ 5 oz. units
Termination date: Jan 12, 2017
Reason for recall: Cranberry Orange Scones are recalled because they may contain undeclared Milk, Egg, Soy, and Wheat.
Voluntary / mandated: Voluntary: Firm initiated
Product description: 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 back of the package.
Distribution pattern: distributed in WA
Recall initiation date: Dec 14, 2016
Initial firm notification: Press Release
Center classification date: Dec 28, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1085-2017, published Jan 4, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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