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Recall for Software Chip of da Vinci S, Intuitive Surgical PDF, 126KB, File does not meet accessibility standards Date: 30. September 2008 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03407/08

Safety Notice for Pulsera and Endura, Philips PDF, 87KB, File does not meet accessibility standards Date: 30. September 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03457/08

Safety Notice for BV Pulsera and Endura, Philips PDF, 93KB, File does not meet accessibility standards Date: 30. September 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03458/08

Safety Notice for EasyVision/RAD, Philips PDF, 84KB, File does not meet accessibility standards Date: 30. September 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02320/08

Safety Notice for Advantage Workstation Suite-Card IQ, GE Healthcare PDF, 101KB, File does not meet accessibility standards Date: 30. September 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02296/08

Recall for PALL High Efficiency In-Process Filter System for Leucocyte Removal from Pooled Buffy Coat Platelets, Pall PDF, 111KB, File does not meet accessibility standards Date: 29. September 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02083/08

Safety Notice for Zeus anaesthesia machine, Dräger PDF, 137KB, File does not meet accessibility standards Date: 29. September 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03422/08

Information for HD3 Ultrasound Systems, Philips PDF, 144KB, File does not meet accessibility standards Date: 29. September 2008 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 03260/08

Medical Device Correction for HDI4000 Ultrasound Systems, Philips PDF, 169KB, File does not meet accessibility standards Date: 29. September 2008 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 03261/08

Recall for Biatin-Ibu Non-Adhesive Foam Dressing, Coloplast PDF, 61KB, File does not meet accessibility standards Date: 29. September 2008 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 03301/08

Recall for Nitinol guide wire, OptiMed PDF, 149KB, File does not meet accessibility standards Date: 18. September 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03401/08

Safety Notice for Beatle/Puma - Restraint system for transportation, Handicare PDF, 66KB, File does not meet accessibility standards Date: 18. September 2008 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02746/08

Recall for Bone marrow aspiration / biopsy puncture needle, trocar 3,00 mm, OptiMed PDF, 84KB, File does not meet accessibility standards Date: 18. September 2008 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03408/08

Corrective action for Trugene HIV-1 GuideLines Rules 12.0 and 11.0, Siemens PDF, 159KB, File does not meet accessibility standards Date: 18. September 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03312/08

Corrective Action Trugene HIV-1 GuideLines Rules 13.0, Siemens PDF, 159KB, File does not meet accessibility standards Date: 18. September 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03312/08

Corrective action for MicroScan Dried Overnight Gram Negative and Synergies plus Negative Panels, Siemens PDF, 102KB, File does not meet accessibility standards Date: 18. September 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03289/08

Recall/Corrective action for Varelisa U1RNP Antibodies Kit, Phadia PDF, 10KB, File does not meet accessibility standards Date: 17. September 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03142/08

Recall for ΩConnector, HEINZ KURZ PDF, 30KB, File does not meet accessibility standards Date: 17. September 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03068/08

Advisory Notice for syngo CT 2007S SP3, Siemens PDF, 59KB, File does not meet accessibility standards Date: 17. September 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03115/08

Safety Notice for MOSAIQ, IMPAC PDF, 23KB, File does not meet accessibility standards Date: 17. September 2008 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03296/08

Recall / Corrective Action for m2000sp Instrument, Abbott PDF, 83KB, File does not meet accessibility standards Date: 17. September 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03185/08

Recall for Cleartest Troponin I, Servoprax PDF, 276KB, File does not meet accessibility standards Date: 15. September 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03316/08

Corrective Action for Responder 2000 Defibrillator, MDSS PDF, 76KB, File does not meet accessibility standards Date: 15. September 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03011/08

Recall for Stat Profile CCX Creatinine Membrane Kits, Nova Biomedical PDF, 185KB, File does not meet accessibility standards Date: 15. September 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03279/08

Safety Notice for Avantgarde Back Tube, Otto Bock PDF, 53KB, File does not meet accessibility standards Date: 15. September 2008 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 00829/07

Safety Notice for Axiom Artis systems, Siemens PDF, 95KB, File does not meet accessibility standards Date: 15. September 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03290/08

Safety Notice for Model 3387, 3387S, 3389 and 3389S, Deep Brain Stimulation (DBS) Lead Kits, Medtronic PDF, 351KB, File does not meet accessibility standards Date: 12. September 2008 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03054/08

Information for Recalibration of the Command Modules 90496 and 91496, Spacelabs Healthcare PDF, 27KB, File does not meet accessibility standards Date: 12. September 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03204/08

Recall for TOPRO Olympos rollator, Handicare PDF, 55KB, File does not meet accessibility standards Date: 12. September 2008 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 03258/08

Recall for Wallaby III Tibial insert C-18 and B-18, constrained, Zimmer PDF, 75KB, File does not meet accessibility standards Date: 11. September 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02604/08