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Recall for ON-Q elastomeric pumps with an integrated bolus component ONDEMAND, I-Flow PDF, 52KB, File does not meet accessibility standards Date: 17. November 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03819/09

Recall CO2–based cryosurgical instruments, Wallach Surgical Devices PDF, 76KB, File does not meet accessibility standards Date: 16. November 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03660/09

Information for PENTRA 400 Software, Horiba Medical PDF, 206KB, File does not meet accessibility standards Date: 16. November 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03668/09

Safety Notice for WM-P1, WM-260 and WM-SC ranges of mobile workstation trolleys, Olympus KeyMed PDF, 92KB, File does not meet accessibility standards Date: 13. November 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02497/09

Recall for Incor LVAD, Berlin Heart GmbH PDF, 43KB, File does not meet accessibility standards Date: 13. November 2009 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 04007/09

Recall Information for defected motors in Dialysis-Chairs and Dialysis-Bed-Chairs, Likamed PDF, 43KB, File does not meet accessibility standards Date: 13. November 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02776/09

Recall for Imager™ II Angiographic Catheters and Imager™ II Urology Torque Catheters, Boston Scientific PDF, 481KB, File does not meet accessibility standards Date: 13. November 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04096/09

Corrective action of certain automated external defibrillators (AEDs), Cardiac Science Corp. PDF, 50KB, File does not meet accessibility standards Date: 12. November 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03897/09

Safety Notice for Active Cortisol ELISA, Beckman Coulter PDF, 100KB, File does not meet accessibility standards Date: 11. November 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02794/09

Safety Notice for the ApexPro Telemetry System, GE Healthcare PDF, 69KB, File does not meet accessibility standards Date: 10. November 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03971/09

Safety Notice for AXIOM Artis MP, Artis dMP or Artis zee Multi Purpose, Siemens PDF, 190KB, File does not meet accessibility standards Date: 10. November 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02646/09

Recall for Genesis II C/R Femoral Size 8 Right, Smith & Nephew PDF, 79KB, File does not meet accessibility standards Date: 10. November 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03322/09

Recall SN connector, article 1703, Serumwerk Bernburg PDF, 77KB, File does not meet accessibility standards Date: 10. November 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03257/09

Safety Notice for Bicarbonate FS, DiaSys Diagnostic Systems PDF, 43KB, File does not meet accessibility standards Date: 09. November 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03887/09

Recall for Thoratec HeartMate II and HeartMate XVE LVAS, Thoratec Corp. PDF, 298KB, File does not meet accessibility standards Date: 09. November 2009 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03850/09

Recall for Quatrix® Aspheric Evolutive Yellow IOL, Croma Pharma PDF, 121KB, File does not meet accessibility standards Date: 06. November 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03890/09

Corrective Action for von Willebrand Reagent, Siemens PDF, 114KB, File does not meet accessibility standards Date: 06. November 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03722/09

Safety Notice for ASX control unit, Novacare PDF, 66KB, File does not meet accessibility standards Date: 06. November 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 03899/09

Corrective action for Responder 2000 defibrillator/monitor, Cardiac Science Corp. PDF, 77KB, File does not meet accessibility standards Date: 05. November 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04003/08

Recall for HeartStart FR2, Philips PDF, 95KB, File does not meet accessibility standards Date: 05. November 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03756/09

Safety Notice: 4D Integrated Treatment Console, Varian Medical PDF, 221KB, File does not meet accessibility standards Date: 05. November 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03797/09

Safety Notice for Centricity Enterprise Archive, GE Healthcare PDF, 153KB, File does not meet accessibility standards Date: 05. November 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03782/09

Safety Notice for syngo Workflow MLR, Siemens PDF, 99KB, File does not meet accessibility standards Date: 04. November 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03494/09

Safety Notice for Pedicel Screwdriver-Set OASYS, Weber Instrumente PDF, 73KB, File does not meet accessibility standards Date: 04. November 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03827/09

Safety Notice for TACSI Bloodcentrifuge, A. Hettich GmbH & Co. KG PDF, 49KB, File does not meet accessibility standards Date: 04. November 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03810/09

Information for Compat Go and Compat Go Plus pumps, Nestlé Healthcare Nutrition PDF, 93KB, File does not meet accessibility standards Date: 04. November 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03378/09

Safety Notice for Durom Acetabular Cup, Zimmer PDF, 2MB, File does not meet accessibility standards Date: 03. November 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02805/09

Recall for Kent Hip Twist Drills, Biomet PDF, 206KB, File does not meet accessibility standards Date: 03. November 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03745/09

Recall for Vitrax II, Ophthalmic Viscosurgical Devices (Sodium Hyaluronate 3%)", 0,65 ml, Abbott PDF, 158KB, File does not meet accessibility standards Date: 03. November 2009 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 03965/09

Recall for Vapotherm Precision Flow®, Disposable Patient Circuit, RMS PDF, 135KB, File does not meet accessibility standards Date: 03. November 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03888/09