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14,972 results

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Safety Notice for the KIMVENT* Closed Suction Systems, Halyard Health PDF, 295KB, File does not meet accessibility standards Date: 21. September 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 06136/15

Safety Notice for the Brilliance 64 and Ingenuity CT Scanners, Philips Healthcare PDF, 55KB, File does not meet accessibility standards Date: 21. September 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 06356/15

Safety Notice regarding MCS-Port Obturator / MCS5000, A. M. I. Agency for Medical Innovations GmbH PDF, 66KB, File does not meet accessibility standards Date: 21. September 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 06611/15

Recall for the Aliquot Delivery Kits (Syringe and Plunger), Stryker® Orthobiologics PDF, 55KB, File does not meet accessibility standards Date: 21. September 2015 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - auxiliary equipment
Reference 06209/15

Safety Corrective Action/Recall for PORT-A-CATH® Plastic Hub Needles, Smiths Medical PDF, 242KB, File does not meet accessibility standards Date: 21. September 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - injection kits
Reference 06681/15

Important Safety Notice for the XiO RTP System, IMPAC Medical Systems, Inc. PDF, 35KB, File does not meet accessibility standards Date: 21. September 2015 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 06197/15

Important Information for the Accu-Chek Insight system, Roche Diabetes Care PDF, 200KB, File does not meet accessibility standards Date: 21. September 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 05446/15

Corrective action for the Valved Entry Systems sold as stand-alone, within CONSTELLATION® TOTALPLUS® Paks, and within Alcon CUSTOM-PAKS, Alcon Laboratories Inc. PDF, 130KB, File does not meet accessibility standards Date: 21. September 2015 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 05402/15

Recall for the ThruPort™ Knot Pusher Model KP1 and Valve Placement Pack Model VPP, Edwards Lifesciences LLC PDF, 52KB, File does not meet accessibility standards Date: 16. September 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - cardiac/thorax surgery
Reference 06311/15

Recall for the Actifuse ABX, Actifuse MIS System and Inductigraft products, Baxter Healthcare Corporation PDF, 175KB, File does not meet accessibility standards Date: 16. September 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - materials for implants
Reference 06062/15

Corrective action for the iChemVELOCITY Urine Chemistry Strips, Iris International PDF, 199KB, File does not meet accessibility standards Date: 16. September 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05794/15

Urgent Safety Notice for the Neptune® 2 Docker (STRYKER NEPTUNE® 2 WASTE MANAGEMENT SYSTEM), Stryker Instruments PDF, 454KB, File does not meet accessibility standards Date: 16. September 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05963/15

Recall for the Idylla™ KRAS Mutation Test, Biocartis PDF, 3MB, File does not meet accessibility standards Date: 16. September 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 04931/15

Urgent Safety Notice for the Digital Radiography X-Ray Systems DR 400, Agfa Healthcare N.V. PDF, 35KB, File does not meet accessibility standards Date: 16. September 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 06049/15

Recall for the product Genu Arexa, Otto Bock HealthCare GmbH PDF, 241KB, File does not meet accessibility standards Date: 15. September 2015 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - orthoses
Reference 06029/15

Urgent Safety Notice for the Medtronic CryoConsole, Medtronic PDF, 42KB, File does not meet accessibility standards Date: 15. September 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 06259/15

Urgent Safety Notice for the Cuff Controller (Shiley Pressure Control), VBM Medizintechnik GmbH PDF, 2MB, File does not meet accessibility standards Date: 15. September 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electronic blood pressure monitor
Reference 06026/15

Urgent Safety Notice for Neopterin EIA, Brahms GmbH PDF, 118KB, File does not meet accessibility standards Date: 10. September 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 05647/15

Field Safety Notice for Flexi-Slip™ Endotracheal Tube Stylet, Teleflex Medical PDF, 311KB, File does not meet accessibility standards Date: 10. September 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05980/15

Corrective action for the product Nit-Occlud Implantation Sheath, pfm medical mepro gmbh PDF, 2MB, File does not meet accessibility standards Date: 03. September 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 05106/15

Urgent Safety Notice for the Cholesterol FS, Creatinine PAP FS and for the other tests based on trinder reactions, DiaSys Diagnostic Systems GmbH PDF, 101KB, File does not meet accessibility standards Date: 03. September 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04289/15

Recall for the silicon tube 1008, Hippokratec GmbH PDF, 22KB, File does not meet accessibility standards Date: 03. September 2015 Topics: Medical devices Type: Customer information

Product group Physical therapy - insufflation technique
Reference 04532/15

Urgent Safety Notice for the ceiling pendants SPR10, MZ Liberec a.s. PDF, 2MB, File does not meet accessibility standards Date: 03. September 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04576/15

Urgent Safety Notice for the MICTEC Hook electrode, DUFNER Instrumente GmbH PDF, 2MB, File does not meet accessibility standards Date: 02. September 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 05254/15

Urgent Safety Notice for Hitachi MRI Systems AIRIS Vento, AIRIS Vento LT, APERTO Eterna, APERTO Lucent, Echelon and Oasis, Hitachi Medical Corporation PDF, 249KB, File does not meet accessibility standards Date: 02. September 2015 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 05943/15

Urgent Safety Notice for the JenaValve prosthesis, JenaValve Technology GmbH PDF, 172KB, File does not meet accessibility standards Date: 02. September 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - cardiac surgery
Reference 04283/15

Corrective action for RUSSKA Rollator Standard and Rollator Aluminium, Ludwig Bertram GmbH PDF, 34KB, File does not meet accessibility standards Date: 02. September 2015 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - daily living aids
Reference 05527/15

Corrective action for the Covidien Medi-Trace™ Cadence Adult Multi-Function Defibrillation Electrodes, Covidien/Medtronic PDF, 115KB, File does not meet accessibility standards Date: 02. September 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 06034/15

Safety Notice for the METHA Titanium Cone Adapter (Neck), Aesculap AG PDF, 407KB, File does not meet accessibility standards Date: 02. September 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05799/15