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Name Date Date initiated Country Source
Recall of Device Recall Gemini, Alaris 2007-06-18 United States USFDA
Recall of Device Recall Microcuff 2007-06-04 United States USFDA
Recall of Device Recall Microcuff 2007-06-04 United States USFDA
Recall of Device Recall Zyoptix XP Epi Separator 2007-06-08 United States USFDA
Recall of Device Recall LIFEPAK 500 2007-06-13 United States USFDA
Recall of Device Recall OEC 9900 Elite MD Motorized CArm System 2007-03-01 United States USFDA
Recall of Kendall 2004-10-08 United States USFDA
Recall of Device Recall OEC 9800 MD Motorized CArm System 2007-03-01 United States USFDA
Recall of Device Recall IL 2007-06-19 United States USFDA
Recall of Device Recall Kodak Direct View DR 7500 System 2007-03-06 United States USFDA
Recall of Device Recall HeartStart XL 2007-06-11 United States USFDA
Recall of Device Recall AngioJet XVG Thrombectomy Catheter 2007-06-19 United States USFDA
Recall of Device Recall Kodak Direct View DR3000 System 2007-03-06 United States USFDA
Recall of Device Recall PhaSeal Intravascular Administration Set 2007-06-26 United States USFDA
Recall of Device Recall PhaSeal Intravascular Administration Set 2007-06-26 United States USFDA
Recall of Device Recall HillRom VersaCare 2006-11-12 United States USFDA
Recall of Device Recall 4Closure Surgical Fascia 2007-06-19 United States USFDA
Recall of Device Recall 4Closure Surgical Fascia 2007-06-19 United States USFDA
Recall of Device Recall 4Closure Surgical Fascia 2007-06-19 United States USFDA
Recall of Device Recall 4Closure Surgical Fascia 2007-06-19 United States USFDA
Recall of Device Recall 4Closure Surgical Fascia 2007-06-19 United States USFDA
Recall of Device Recall 4Closure Surgical Fascia 2007-06-19 United States USFDA
Recall of Device Recall Brilliance CT Systems 2007-05-25 United States USFDA
Recall of Device Recall Brilliance CT Systems 2007-05-25 United States USFDA
Recall of Device Recall PhaSeal Intravascular Administration Set 2007-06-26 United States USFDA