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Safety Notice for the HexaPOD evo RT System, Medical Intelligence Medizintechnik GmbH PDF, 291KB, File does not meet accessibility standards Date: 24. June 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03096/14

Corrective action for the product Enzygnost Syphilis, Siemens PDF, 60KB, File does not meet accessibility standards Date: 23. June 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 03040/14

Update to the global Field Corrective Action for the Standard Offset Cup Impactor, Greatbatch Medical PDF, 234KB, File does not meet accessibility standards Date: 20. June 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00694/14

Safety Notice for the LANTIS™ OIS system, Siemens PDF, 636KB, File does not meet accessibility standards Date: 20. June 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 02577/14

Corrective action for the HeartWare® Ventricular Assist System, HeartWare, Inc. PDF, 214KB, File does not meet accessibility standards Date: 20. June 2014 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 02492/14

Corrective action for the Vivid E9 ultrasound systems and probes C1-5-D, C2-9-D, IC5-9-D, and M5Sc-D, GE Healthcare PDF, 71KB, File does not meet accessibility standards Date: 20. June 2014 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 02481/14

Corrective action for syngo® RT Therapist 4.3.SP1 and syngo® RT Oncologist 4.3.SP1, Siemens PDF, 13KB, File does not meet accessibility standards Date: 20. June 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 03223/14

Safety Information for the monopolar hook electrode, Gebrüder Martin GmbH & Co. KG PDF, 2MB, File does not meet accessibility standards Date: 20. June 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 03181/14

Corrective action for the product DF53C GS CorPatch easy pre-connected with 1.3m cable, Leonhard Lang Medizintechnik PDF, 187KB, File does not meet accessibility standards Date: 20. June 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02399/14

Recall for Mentor® Gel Sizers, Mentor Medical Systems B.V. PDF, 467KB, File does not meet accessibility standards Date: 18. June 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03122/14

Corrective action for the FUJIFILM Digital Mammography System AMULET, FUJIFILM PDF, 355KB, File does not meet accessibility standards Date: 18. June 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for mammographic diagnostics
Reference 03175/14

Follow-Up Urgent Safety Notice for the UniCel DxI Immunoassay Systems, Beckman Coulter PDF, 27KB, File does not meet accessibility standards Date: 18. June 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06525/13

Corrective action for the NAV3i Platforms and Power Box, Stryker PDF, 85KB, File does not meet accessibility standards Date: 18. June 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03069/14

Corrective action for the NOxBOXi Inhaled Nitric Oxid Delivery and Monitoring Device, Bedfont Scientific Ltd. PDF, 1MB, File does not meet accessibility standards Date: 18. June 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 02941/14

Corrective action for the Integral Leg Prosthesis, Orthodynamics GmbH PDF, 49KB, File does not meet accessibility standards Date: 18. June 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 01696/12

Corrective action for the RAPIDPoint® 500 System, Siemens PDF, 23KB, File does not meet accessibility standards Date: 18. June 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03171/14

Recall of SUTUREFIX Ultra Anchors, Smith & Nephew PDF, 69KB, File does not meet accessibility standards Date: 17. June 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03131/14

Urgent Safety Notice for the Alere Triage® BNP Calibrator for the Beckman Coulter Access Family of Immunoassay Systems, Alere San Diego, Inc. PDF, 152KB, File does not meet accessibility standards Date: 17. June 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 03176/14

Corrective action for Dual mobility acetabular cup SATURNE®, Amplitude GmbH PDF, 53KB, File does not meet accessibility standards Date: 17. June 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 02860/14

Corrective action for Navigation Software Spine & Trauma 3D 2.0 and 2.1, Brainlab AG PDF, 831KB, File does not meet accessibility standards Date: 17. June 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - navigation systems
Reference 03232/14

Recall for the product i-Visc 1.4, i-Medical Ophthalmic International GmbH PDF, 2MB, File does not meet accessibility standards Date: 17. June 2014 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - liquid media for ophthalmological purposes
Reference 00176/12

Urgent Safety Notice for the Fraxel DUAL 1550/1927 Laser System, Solta Medical Inc. PDF, 180KB, File does not meet accessibility standards Date: 16. June 2014 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - laser technology
Reference 02123/14

Safety Notice for the STIMPOD Neuromuscular Stimulator, Xavant Technology PDF, 71KB, File does not meet accessibility standards Date: 16. June 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 01865/14

Corrective action for the Ingenia, Intera, Achieva and Multiva MR Systems using R5.1 .1 and R5.1.2 version of software, Philips Healthcare PDF, 226KB, File does not meet accessibility standards Date: 16. June 2014 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 03022/14

Corrective action for the Oxoid Antimicrobial Susceptibility Testing Disc P1 Penicillin G, Thermo Fisher Scientific Microbiology Basingstoke / Oxoid Ltd. PDF, 18KB, File does not meet accessibility standards Date: 16. June 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 02578/14

Batch Recall of ELS Syringes, PEROUSE MEDICAL PDF, 69KB, File does not meet accessibility standards Date: 16. June 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 00313/14

Corrective action for the Hamilton Galileo Ventilator Flexport, Spacelabs Healthcare PDF, 53KB, File does not meet accessibility standards Date: 16. June 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 03235/14

Corrective action for MiniCap Extended Life PD Transfer Set with Twist Clamp, Baxter PDF, 38KB, File does not meet accessibility standards Date: 13. June 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 02666/14

Synthes GmbH: Safety Notice for the Orbital Rim Plate, 1.3 curved, 9 holes, Pure Titan PDF, 6MB, File does not meet accessibility standards Date: 13. June 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 02998/14