FDA Recall Sensodyne Complete Protection
View Recall Number, Date, Reasons, Quantity
FDA Recall Enforcement Reports
The last Recall Enforcement Report for Sensodyne Complete Protection with NDC 0135-0573 was initiated on 07-15-2015 as a Class II recall due to presence of foreign substance: fragments of wood found when the product was extruded onto a toothbrush. The latest recall number for this product is D-1322-2015 and the recall is currently terminated as of 04-19-2017 .
| Recall Number | Initiation Date | Report Date | Recall Classification | Product Quantity | Product Description | Status |
|---|---|---|---|---|---|---|
| D-1322-2015 | 07-15-2015 | 08-19-2015 | Class II | 81,376 tubes | 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 | Terminated |
| D-1321-2015 | 07-15-2015 | 08-19-2015 | Class II | 50,860 tubes | SENSODYNE EXTRA FRESH 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 0135-0572-02 | Terminated |
What is the Enforcement Report?
All drug recalls are monitored by the Food and Drug Administration (FDA) and are included in the Enforcement Report once they are properly classified. The FDA will determine if a firm's removal or correction actions of a marked product meet the requirements to be considered a "recall". The FDA will also determine the public hazard assessment and a recall classification will be published in the Enforcement Report.