PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: August 19, 2015 Initiated: July 15, 2015 #D-1322-2015

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.

Details

Units Affected
81,376 tubes
Distribution
Nationwide, Puerto Rico & Taiwan
Location
Moon Township, PA

Frequently Asked Questions

What product was recalled?
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. Recalled by GlaxoSmithkline Consmer Healthcare. Units affected: 81,376 tubes.
Why was this product recalled?
Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 19, 2015. Severity: Moderate. Recall number: D-1322-2015.