Mode Liste Mode Grille
Nom Date Date de mise en oeuvre Pays Source
Rappel de Device Recall PERPOS PLS SYSTEM 2011-03-23 United States USFDA
Rappel de Device Recall KyphoPak Express Tray First Fracture, 15/2 with KyphX Osteo Introducer System 2011-03-23 United States USFDA
Rappel de Device Recall PERPOS PLS System Single Use 2011-02-03 United States USFDA
Rappel de Device Recall Reusable BONELOK PLS System; 2011-02-03 United States USFDA
Rappel de Device Recall PERPOS Driver 2011-02-03 United States USFDA
Rappel de Device Recall PERPOS PLS SYSTEM 2011-03-23 United States USFDA
Rappel de Device Recall BONELOK PLS Implant 2011-03-15 United States USFDA
Rappel de Device Recall Orthovita(R) Cortoss(TM) Delivery Gun 2011-03-31 United States USFDA
Rappel de Device Recall Pathfinder NXT Closure Top Driver Long 2011-05-20 United States USFDA
Rappel de Device Recall Pathfinder NXT Closure Top Driver Short 2011-05-20 United States USFDA
Rappel de Device Recall Biomet CC IBeam Tibial Plate 75mm 2011-03-03 United States USFDA
Rappel de Zimmer Trabecular Metal Modular Acetabular System 2011-09-01 United States USFDA
Rappel de ZMR Porous Revision Hip Prosthesis and ZMR Revision Taper Hip Prosthesis 2011-10-21 United States USFDA
Rappel de ZMR Porous Revision Hip Prosthesis and ZMR Revision Taper Hip Prosthesis 2011-10-21 United States USFDA
Rappel de ZMR Porous Revision Hip Prosthesis and ZMR Revision Taper Hip Prosthesis 2011-10-21 United States USFDA
Rappel de ZMR Porous Revision Hip Prosthesis and ZMR Revision Taper Hip Prosthesis 2011-10-21 United States USFDA
Rappel de ANCHORLOK 2011-09-20 United States USFDA
Rappel de ANCHORLOK 2011-09-20 United States USFDA
Rappel de ANCHORLOK 2011-09-20 United States USFDA
Rappel de ANCHORLOK 2011-09-20 United States USFDA
Rappel de ANCHORLOK 2011-09-20 United States USFDA
Rappel de ANCHORLOK 2011-09-20 United States USFDA
Rappel de ANCHORLOK 2011-09-20 United States USFDA
Rappel de ANCHORLOK 2011-09-20 United States USFDA
Rappel de ANCHORLOK 2011-09-20 United States USFDA