D-1322-2015 Class II Terminated
FDA drug recall D-1322-2015 was initiated by GlaxoSmithkline Consmer Healthcare on July 15, 2015 and is designated Class II. Reason for recall: Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush. The recall status is terminated (terminated April 19, 2017). Affected quantity: 81,376 tubes.
Recall Details
- Product Type
- Drugs
- Report Date
- August 19, 2015
- Initiation Date
- July 15, 2015
- Termination Date
- April 19, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 81,376 tubes
Product Description
SENSODYNE COMPLETE PROTECTION, 3.4 oz. (96.4 g)tubes, Manufactured by Oratech, South Jordan UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108, NDC 0135-0573-02
Reason for Recall
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Distribution Pattern
Nationwide, Puerto Rico & Taiwan
Code Information
Lot # B4D031, Exp 03/16 B4E101, Exp 04/16 B4F261,B4F291,B4G011, Exp 05/16 B4G031, B4G091, Exp 06/16 B4J031, Exp 07/16