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Safety Notice for Primedic™ HeartSave Series, Metrax GmbH PDF, 51KB, File does not meet accessibility standards Date: 01. March 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00597/10

Recall for Hydrolift insertion instrument with Hydrolift hydraulic pipe, Aesculap AG PDF, 47KB, File does not meet accessibility standards Date: 26. February 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00442/10

Recall for Dimension Vista ECREA Flex Reagent cartridges, Siemens PDF, 58KB, File does not meet accessibility standards Date: 26. February 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00622/10

Recall for SafeSheath® CSG® Coronary Sinus Guide Hemostatic Introducer System with Infusion Sideport, Thomas Medical PDF, 216KB, File does not meet accessibility standards Date: 26. February 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00295/10

Renewed Recall for Input TS Introducer Sets with Needle, Medtronic PDF, 48KB, File does not meet accessibility standards Date: 25. February 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03832/08

Recall for Novy Cornual Cannulation Set, Cook PDF, 75KB, File does not meet accessibility standards Date: 25. February 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00250/10

Safety Information for COBAS AmpliPrep R-Tips, Roche PDF, 157KB, File does not meet accessibility standards Date: 25. February 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00361/10

Recall for Access Immunoassay System AccuTnI Reagent Kit, Beckman Coulter PDF, 87KB, File does not meet accessibility standards Date: 25. February 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00544/10

Recall for Grafix Tendon Stripper, ConMed Linvatec PDF, 88KB, File does not meet accessibility standards Date: 24. February 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00458/10

Another Information for Galileo Cervical Disc Prosthesis, Signus PDF, 908KB, File does not meet accessibility standards Date: 24. February 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02712/09

Corrective Action for Paraffin Pretreatment Reagent Kit II and Paraffin Pretreatment Reagent Kit III, Abbott PDF, 130KB, File does not meet accessibility standards Date: 24. February 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00437/10

Safety Notice: Instructions for Use Modification for VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Maquet PDF, 43KB, File does not meet accessibility standards Date: 23. February 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 00331/10

Safety Notice: Update of the Implant Extraction Set Brochure, Stryker PDF, 62KB, File does not meet accessibility standards Date: 23. February 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00451/10

Safety Notice for MultiPlan® Treatment Planning System, Accuray PDF, 54KB, File does not meet accessibility standards Date: 22. February 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 00346/10

Corrective Action for UniMatch Software v4.01, Invitrogen PDF, 1MB, File does not meet accessibility standards Date: 22. February 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04814/09

Safety Notice concerning T-Pieces, Intersurgical PDF, 208KB, File does not meet accessibility standards Date: 22. February 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00344/10

Corrective Action for TCAutomation/enGen Laboratory Automation Systems, Thermo Fisher Scientific PDF, 119KB, File does not meet accessibility standards Date: 19. February 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00398/10

Corrective Action for Analyzers ABL505/555, EML105, ABL600, ABL700 Series, ABL800FLEX and ABL800BASIC, Radiometer PDF, 50KB, File does not meet accessibility standards Date: 19. February 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00169/10

Safety Notice for Powerheart 9300A, 9300E, 9300P, 9390A, 9390E and Responder model 2023440, Cardiac Science PDF, 60KB, File does not meet accessibility standards Date: 19. February 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00438/10

Lot Recall for Vitesse Biopsie Needle, Delta-Cut, 2-part, OptiMed PDF, 151KB, File does not meet accessibility standards Date: 19. February 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00473/10

Safety Notice for EnRhythm, EnRhythm MRI and Advisa pacemakers, Medtronic PDF, 156KB, File does not meet accessibility standards Date: 18. February 2010 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 00475/10

Safety Notice for Basic T1 perfusion package, Philips PDF, 64KB, File does not meet accessibility standards Date: 18. February 2010 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 04717/09

Recall for Oxidase Identification Sticks, OXOID Ltd. /Thermo Fisher Scientific PDF, 59KB, File does not meet accessibility standards Date: 18. February 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00254/10

Safety Notice / Recall for TPHA Test kit, Oxoid Ltd. PDF, 40KB, File does not meet accessibility standards Date: 17. February 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00272/10

Corrective Action for SYNCHRON LXi 725 and UniCel DxC 600i Systems, Beckman Coulter PDF, 90KB, File does not meet accessibility standards Date: 16. February 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00441/10

Information for Thermoflect, TechStyles PDF, 116KB, File does not meet accessibility standards Date: 16. February 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04933/09

Information for Laryngoscope Handle, Medida PDF, 48KB, File does not meet accessibility standards Date: 16. February 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 04626/09

Recall for CD 103 PE and CD 103 FITC reagents, Becton Dickinson PDF, 81KB, File does not meet accessibility standards Date: 16. February 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00151/10

Field Safety Notice for the Harness Safety System, Maquet PDF, 41KB, File does not meet accessibility standards Date: 10. February 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04596/09

Information for handholds delivered by Rolko, Hill Rom PDF, 65KB, File does not meet accessibility standards Date: 10. February 2010 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 00019/10