Z-0859-2012 Class II Terminated
FDA device recall Z-0859-2012 was initiated by Church & Dwight Inc on December 22, 2011 and is designated Class II. Reason for recall: Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life. The recall status is terminated (terminated April 14, 2015). Affected quantity: 15.589 million units.
Recall Details
- Product Type
- Devices
- Report Date
- August 8, 2012
- Initiation Date
- December 22, 2011
- Termination Date
- April 14, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 15.589 million units
Product Description
Arm and Hammer Spinbrush Dual Action Powered Toothbrush Spinbrush Pro Whitening Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.
Reason for Recall
Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.
Distribution Pattern
Worldwide Distribution.
Code Information
N/A