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Safety Notice for Signa 3T Magnetic Resonance Systems, GE Healthcare PDF, 64KB, File does not meet accessibility standards Date: 11. August 2009 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 01628/08

Recall for BHR Acetabular Cups, Smith & Nephew PDF, 663KB, File does not meet accessibility standards Date: 10. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02307/09

Recall for GALILEO Cervical Disc Prosthesis, SIGNUS MEDIZINTECHNIK GmbH PDF, 168KB, File does not meet accessibility standards Date: 10. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02712/09

Recall for 4Z1c Matrix Array Transducer on the ACUSON SC2000, Siemens PDF, 78KB, File does not meet accessibility standards Date: 10. August 2009 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 02706/09

Safety Notice for Angiostar, Multistar, Neurostar, Coroskop and Bicor systems, Siemens PDF, 491KB, File does not meet accessibility standards Date: 10. August 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01303/09

Recall for Twin-Pass® Dual Access Catheter, Vascular Solutions PDF, 125KB, File does not meet accessibility standards Date: 07. August 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02538/09

Safety Notice for Hedrin, Pouxit, Silikom, Etopril and XT Luis, Thornton & Ross PDF, 88KB, File does not meet accessibility standards Date: 05. August 2009 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 04774/08

Recall for PERIMOUNT aortic, PERIMOUNT Plus, PERIMOUNT Magna Ease valves, Edwards Lifesciences PDF, 137KB, File does not meet accessibility standards Date: 05. August 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04519/08

Safety Notice for Centricity PACS RA1000 Workstation; Software: 2.1.x and 3.0.x, GE Healthcare PDF, 142KB, File does not meet accessibility standards Date: 05. August 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02412/09

Safety Notice for Centricity PACS RA1000 Workstation; Software: PathSpeed 7.x, 8.x, Centricity 1.X, 2.0.X, GE Healthcare PDF, 142KB, File does not meet accessibility standards Date: 05. August 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02412/09

Safety Notice for Centricity PACS RA1000 Workstation Software, GE Healthcare PDF, 76KB, File does not meet accessibility standards Date: 04. August 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02412/09

Safety Notice for Centricity PACS RA1000 Workstation Software, GE Healthcare PDF, 76KB, File does not meet accessibility standards Date: 04. August 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02412/09

Addendum of the lot recall of Formoline L112, Certmedica PDF, 64KB, File does not meet accessibility standards Date: 04. August 2009 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 02977/08

Safety Notice for Alaris GP Volumetric Pumps and Alaris GP Guardrails Volumetric Pumps, Cardinal Health PDF, 40KB, File does not meet accessibility standards Date: 04. August 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02140/09

Safety Notice for GCX Euro Rail Clamp, Dräger Medical PDF, 185KB, File does not meet accessibility standards Date: 31. July 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02606/08

Safety Notice for TheraScreen EGFR29 Mutation Kit, DxS Ltd. PDF, 127KB, File does not meet accessibility standards Date: 31. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01909/09

Field Correction Notice for all e360 ventilators, Newport Medical PDF, 93KB, File does not meet accessibility standards Date: 31. July 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02598/09

Safety Notice for Focal Treatment Planning Software, CMS Software PDF, 98KB, File does not meet accessibility standards Date: 30. July 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02513/09

Recall for Immulite 2000/2500 AlaTOP Allergy Screen Assay, Siemens PDF, 126KB, File does not meet accessibility standards Date: 30. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02645/09

Recall for Isobar TTL-Module In polyaxial screws, SCIENT’X PDF, 223KB, File does not meet accessibility standards Date: 30. July 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02526/09

Extended Recall for Dyonics 25 Tube Sets, Smith & Nephew PDF, 67KB, File does not meet accessibility standards Date: 30. July 2009 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02112/09

Recall for RF Ablation System Foot-Switch, Boston Scientific PDF, 302KB, File does not meet accessibility standards Date: 30. July 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02648/09

Recall of roller blocks for heart-lung-bypass systems, Maquet PDF, 270KB, File does not meet accessibility standards Date: 29. July 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02644/09

Safety Notice for Maxi Move Scoop Stretcher, Arjo Hospital Equipment AB PDF, 210KB, File does not meet accessibility standards Date: 29. July 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02649/09

Safety Notice for Synchrony Respiratory Tracking System, Accuray PDF, 219KB, File does not meet accessibility standards Date: 29. July 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01333/09

Safety Notice for LeVeen™Needle Electrodes, Boston Scientific PDF, 93KB, File does not meet accessibility standards Date: 28. July 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02531/09

Safety Notice for XO 4 Suction tube holder on patient's chair, XO CARE A/S PDF, 115KB, File does not meet accessibility standards Date: 28. July 2009 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 01957/09

Safety Notice for VNS Therapy Model 250 Programming System, Cyberonics PDF, 159KB, File does not meet accessibility standards Date: 28. July 2009 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02605/09

Recall for Birdie Patient Hoist, Invacare Aquatec PDF, 85KB, File does not meet accessibility standards Date: 24. July 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01861/09

Safety Notice for Bright View Gamma Camera, Philips PDF, 98KB, File does not meet accessibility standards Date: 23. July 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02567/09