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  • Device 26490
  • Manufacturer 33665
  • Event 35826
  • Implant 7175
Name Date Date initiated Country Source
Recall of Newport e360 Ventilator 2009-10-27 United States USFDA
Recall of Newport HT70 Ventilator 2010-09-20 United States USFDA
Recall of MAKO PN 204588 Camera 2010-10-25 United States USFDA
Recall of TAPSCOPE 550 2010-10-25 United States USFDA
Recall of Cryostat Microtome, Thermo Scientific Microm HM 550 Cold Disinfection Cryostat 2010-09-23 United States USFDA
Recall of Monaco Radiation Treatment Planning Workstation 2010-10-27 United States USFDA
Recall of Neotrode, Softrade, TruLink 2010-09-23 United States USFDA
Recall of 115V Blanketroll III Model 233 and 115V CoolBlue Model 2501 2010-10-18 United States USFDA
Recall of OmniDiagnost Eleva 2010-10-07 United States USFDA
Recall of MultiDiagnost Eleva 2010-10-07 United States USFDA
Recall of Allura Integris Systems with OMCP Generator 2010-10-07 United States USFDA
Recall of Allura Xper Systems with Velara Generator 2010-10-07 United States USFDA
Recall of Unicel DXC and SYNCHRON LX Clinical Systems 2010-10-22 United States USFDA
Recall of Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Five Lumen Polyurethane 2010-10-04 United States USFDA
Recall of Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Five Lumen Polyurethane 2010-10-04 United States USFDA
Recall of Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Five Lumen Polyurethane 2010-10-04 United States USFDA
Recall of Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Five Lumen Polyurethane 2010-10-04 United States USFDA
Recall of Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Five Lumen Polyurethane 2010-10-04 United States USFDA
Recall of Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Five Lumen Polyurethane 2010-10-04 United States USFDA
Recall of Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Five Lumen Polyurethane 2010-10-04 United States USFDA
Recall of Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Five Lumen Polyurethane 2010-10-04 United States USFDA
Recall of Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Five Lumen Polyurethane 2010-10-04 United States USFDA
Recall of Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Five Lumen Polyurethane 2010-10-04 United States USFDA
Recall of Spectrum Central Venous Catheter Tray, Minocycline/Rifampin Antibiotic Impregnated, 5 Lumen Polyure 2010-10-04 United States USFDA
Recall of Central Venous Catheter Tray Five Lumen Polyurethane 2010-10-04 United States USFDA
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Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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