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Name Date Date initiated Country Source
Recall of Device Recall Bigger BetterBladder 2009-06-03 United States USFDA
Recall of Stryker Atlas Transport Stretcher with Zoom, Model 660Z, Stryker Medical, Portage, MI 2010-03-19 United States USFDA
Recall of Device Recall Stryker MSeries Stretcher 2010-03-19 United States USFDA
Recall of Device Recall Stryker Renaissance Series Stretchers 2010-03-19 United States USFDA
Recall of Device Recall Stryker Renaissance Series Stretchers 2010-03-19 United States USFDA
Recall of Device Recall Stryker power cord kits 2010-03-19 United States USFDA
Recall of Device Recall SwiftLock Anchor, Model 1192 2010-02-22 United States USFDA
Recall of Device Recall Leksell SurgiPlan 2005-05-23 United States USFDA
Recall of Device Recall CELLDYN Emerald Hematology Analyzer System 2010-03-23 United States USFDA
Recall of Device Recall 7.5mm Ti Solid Humeral Nail 230 mm Sterile 2010-02-25 United States USFDA
Recall of Device Recall 7.5mm Ti Solid Humeral Nail 250 mm Sterile 2010-02-25 United States USFDA
Recall of Device Recall EasyRA Cuvette Segments for EasyRA Clinical Chemistry Analyzer 2010-03-29 United States USFDA
Recall of Device Recall Dental chair headrest 2010-03-23 United States USFDA
Recall of Device Recall Continuum Acetabular Systems Shell Inserter Adapter with Rotational Control 2010-03-19 United States USFDA
Recall of Device Recall Continuum Acetabular Systems Shell Inserter Adapter without Rotational Control 2010-03-19 United States USFDA
Recall of Device Recall IILICO MIS Posterior Spinal Fixation System 2011-07-06 United States USFDA
Recall of Device Recall Unicel Synchron Clinical Systems 2010-01-18 United States USFDA
Recall of Device Recall Unicel Synchron Clinical Systems 2010-01-18 United States USFDA
Recall of Device Recall UniCel DxC 880i, 860i,680i and 660i Synchron Access Clinical Systems 2009-05-07 United States USFDA
Recall of Device Recall ARCHITECT HAVABM Reagent 2009-12-30 United States USFDA
Recall of Device Recall COULTER PrepPlus, Part Number: 286600 2010-01-21 United States USFDA
Recall of Device Recall COULTER PrepPlus 2, Part Number: 378600 2010-01-21 United States USFDA
Recall of Device Recall Medtronic HMS PLUS, Hemostasis Management System with Heparin Assay Controls 2010-03-08 United States USFDA
Recall of Device Recall 3D Knee Tibial InsertDCM 2010-03-19 United States USFDA
Recall of Device Recall Beckman Coulter UniCel DxC 880i, 860i, and 600i Systems 2010-02-25 United States USFDA