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Name Date Date initiated Country Source
Recall of Device Recall Arrow Pressure Injectable PICC Kit 2017-03-20 United States USFDA
Recall of Device Recall ETEST Ceftriaxone 2017-01-01 United States USFDA
Recall of Device Recall NMT Patient Cable (989803174581) 2017-05-04 United States USFDA
Recall of Device Recall Willscher Vas Reapproximator Set 2017-05-01 United States USFDA
Recall of Device Recall LATARJET EXPERIENCE Coracoid Top Hat Drill 2017-05-12 United States USFDA
Recall of Device Recall Willscher Vas Skewers 2017-05-01 United States USFDA
Recall of Device Recall Willscher Vas Reapproximator Plate 2017-05-01 United States USFDA
Recall of Device Recall Endoscopic Curved Needle 2017-05-01 United States USFDA
Recall of Device Recall LapSac Introducer 2017-05-01 United States USFDA
Recall of Device Recall LapSac Introducer Set 2017-05-01 United States USFDA
Recall of Device Recall Legacy Full Contour Laboratory Abutment: 3.5mmD Platform/5.5mmD 2017-05-02 United States USFDA
Recall of Device Recall Proteus Plus and Proteus ONE 2017-02-09 United States USFDA
Recall of Device Recall SmartMonitor 2 PS/PSL 2017-05-01 United States USFDA
Recall of Device Recall Mobius 3D 2015-02-23 United States USFDA
Recall of Device Recall Electrophysiology catheter cables 2017-05-08 United States USFDA
Recall of Device Recall Toshiba Angio WorkStation (XIDFAWS801) 2017-02-01 United States USFDA
Recall of Device Recall Nexstim 2017-03-14 United States USFDA
Recall of Device Recall Nexstim 2017-03-14 United States USFDA
Recall of Device Recall Conformer Medium with holes (sterile) 2002-11-29 United States USFDA
Recall of Device Recall Artis zee angiographic xray system 2017-02-03 United States USFDA
Recall of Device Recall Opteryx Variable Rescue Screw 2017-05-05 United States USFDA
Recall of Device Recall Adenovirus (20/11 & 2/6) 2017-05-05 United States USFDA
Recall of Device Recall LeadCare Blood Lead Testing System 2017-05-23 United States USFDA
Recall of Device Recall LeadCare II Blood Lead Testing System 2017-05-23 United States USFDA
Recall of Device Recall Estrogen Receptor (EP1) 2017-05-05 United States USFDA