Mode Liste Mode Grille
Nom Date Date de mise en oeuvre Pays Source
Rappel de Device Recall Baxter Interlink System NonDEHP YType Catheter Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter NonDEHP YType Catheter Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Minivolume Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter NonDEHP I.V. Catheter Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Interlink System NonDEHP Standard Bore 3Lead Catheter Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Interlink System TConnector Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter NonDEHP MicroVolume Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter NonDEHP MicroVolume Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter NonDEHP High Flow Rate Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Stryker PainPump 2006-02-03 United States USFDA
Rappel de Device Recall Baxter Interlink System NonDEHP I.V. Catheter Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter MiniInfuser Microbore Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Anesthesia Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Interlink System Minivolume Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Interlink System Minivolume Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Minivolume Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Interlink System Minivolume Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Interlink System Minivolume Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Interlink System Minivolume Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Interlink System Minivolume Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Interlink System Minivolume Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter NonDEHP Minivolume Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Interlink System Extension Set with Standard Bore 4Way Stopcock Manifold Extension Set and M 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Interlink System 3Lead Extension Set 2005-12-15 United States USFDA
Rappel de Device Recall Baxter Interlink System YType Minivolume Extension Set 2005-12-15 United States USFDA