FDA recall D-1320-2015

GlaxoSmithkline Consmer Healthcare · Class II · drug

Product

biotene PBF Toothpaste (Plaque-Biofilm Loosening Formula), a) 4.3 oz. (121.9 g) tubes, (NDC 0135-0559-01), biotene¿ PBF Paste, b) 4.5 oz.(127.6 g) tubes, (NDC 0135-0490-02), Manufactured by Oratech, South Jordan, UTAH 84095, Distributed by GlaxoSmithKline, Consumer Healthcare, L.P., Moon Township, PA 15108

Reason for recall

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

Distribution

Nationwide, Puerto Rico & Taiwan

Key facts

Status
Terminated
Initiation date
2015-07-15
Report date
2015-08-19
Termination date
2017-04-19
Voluntary/Mandated
Voluntary: Firm initiated
Location
Moon Township, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1320-2015