FDA Drug · D-1322-2015

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

Class II · Terminated

Presence of Foreign Substance: Fragments of wood found when the product was extruded onto a toothbrush.

Affected lots / codes — check yours against thisLot # B4D031, Exp 03/16 B4E101, Exp 04/16 B4F261,B4F291,B4G011, Exp 05/16 B4G031, B4G091, Exp 06/16 B4J031, Exp 07/16

Recalling firm: GlaxoSmithkline Consmer Healthcare, Moon Township, PA
Classification: Class II (temporary or reversible harm possible)
Status: Terminated
Quantity: 81,376 tubes
Distribution: Nationwide, Puerto Rico & Taiwan
Recall initiated: July 15, 2015
Classified: August 11, 2015
Terminated: April 19, 2017
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-1322-2015%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

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