The FDA released a statement against the use of OTC benzocaine teething products due to serious safety risk and lack of benefit. After review of the FDA statement, effective immediately Church & Dwight Co. Inc. (manufacturer) is discontinuing the Medicated Teething Orajel items, and is also treating as a Class II recall (removal of product from the store shelf level).

Please open the attached recall documents to view the detailed information about this recall. The step by step Essbase reporting instructions have been included at the end of the Recall Notification Form.

Click here to view report