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Safety Notice for Discovery VCT, RX VCT, STE, RX and ST PET/CT systems with Dimension console, GE Healthcare PDF, 37KB, File does not meet accessibility standards Date: 01. July 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02506/11

Corrective action of the Surgical Lighting and Media Systems Harmony LA, LC 500 and LA 700, Steris PDF, 185KB, File does not meet accessibility standards Date: 01. July 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01597/11

Recall of several reference and lot numbers of the Coronary Ostia Cannula, Terumo PDF, 45KB, File does not meet accessibility standards Date: 01. July 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02472/11

Recall of the surgical sutures Surgilon, Ticron and Sofsilk, Covidien PDF, 673KB, File does not meet accessibility standards Date: 01. July 2011 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 02689/11

Lot Recall of the Silicone CTS ® (Close to Shaft) Cuff Adjustable Neck Flange Tracheostomy Tubes (Wire reinforced), Arcadia Medical Corporation PDF, 76KB, File does not meet accessibility standards Date: 30. June 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02635/11

Recall of the artificial urinary sphincter “AMS 800 Urinary Control System”, AMS PDF, 108KB, File does not meet accessibility standards Date: 30. June 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02142/11

Safety Notice for Savanah Bath Seats manufactured by Patterson Medical Ltd., RUSSKA PDF, 728KB, File does not meet accessibility standards Date: 30. June 2011 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02609/11

Corrective action for BD Microtrol Candida albicans, Becton Dickinson PDF, 54KB, File does not meet accessibility standards Date: 30. June 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02023/11

Lot Recall of the genitourinary graft Elevate Pelvic Floor Repair Systems with IntePro Lite, AMS PDF, 69KB, File does not meet accessibility standards Date: 29. June 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02144/11

Urgent Safety Notice for ARIA™, Varian medical systems PDF, 323KB, File does not meet accessibility standards Date: 29. June 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02391/11

Lot Recall for the Comprehensive Primary & Fracture Shoulder Stem Inserter, Biomet Orthopaedics PDF, 44KB, File does not meet accessibility standards Date: 29. June 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02405/11

Recall for BOWA electro surgical units ARC 300 and ARC 350, BOWA PDF, 301KB, File does not meet accessibility standards Date: 29. June 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00653/11

Recall for the Mantis Rod Inserter, Stryker Spine Bordeaux PDF, 33KB, File does not meet accessibility standards Date: 29. June 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02728/11

Software error of cranial / ENT Navigation software, BrainLAB AG PDF, 236KB, File does not meet accessibility standards Date: 22. June 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02643/11

Potential pacing inhibition with PARADYM ICDs, Sorin Biomedica CRM S.r.I. PDF, 43KB, File does not meet accessibility standards Date: 22. June 2011 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02002/11

Update of urgent safety information regarding Scorpio T72 Tibia Insert Trials, Stryker Orthopaedics PDF, 167KB, File does not meet accessibility standards Date: 22. June 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02776/10

Safety risk of Artiste digital linear accelerators with syngo® RT Therapist Version 4.1, Siemens Healthcare PDF, 92KB, File does not meet accessibility standards Date: 21. June 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02637/11

Recall of elastomeric AccuFlo infusion pumps, Medpro International Ltd PDF, 157KB, File does not meet accessibility standards Date: 21. June 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01529/11

Possible misassembled plugs in chargers for Echo-Screen / AccuScreen, Natus Europe PDF, 90KB, File does not meet accessibility standards Date: 20. June 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02432/11

Field safety notice concerning malfunction when using syngo plaza with version VA20, Siemens Healthcare PDF, 2MB, File does not meet accessibility standards Date: 20. June 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02130/11

Possible potential interference of Methylene Blue and other vascular dyes with readings on CDI Monitoring Systems, Terumo CardioVascular Systems PDF, 179KB, File does not meet accessibility standards Date: 17. June 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02633/11

Refitting of Spacelabs Medical Capnography Module model 91517, Spacelabs Healthcare PDF, 38KB, File does not meet accessibility standards Date: 17. June 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02519/11

Lot recall of Hemochron Jr. PT Cuvettes, International Technodyne Corporation (ICT) PDF, 63KB, File does not meet accessibility standards Date: 17. June 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02213/11

Incorrect Gantry Angle in Focal Plan Review for XiO IMRT Plans, Elekta CMS PDF, 76KB, File does not meet accessibility standards Date: 17. June 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04098/10

Possible inadvertent deletion of accessory elements (including dynamic MLC) in VARIS Vision, Varian medical systems PDF, 1MB, File does not meet accessibility standards Date: 17. June 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02252/11

Collision risk when lowering table height of Ysio, Siemens Healthcare PDF, 170KB, File does not meet accessibility standards Date: 16. June 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02257/11

Lot Recall for SafeSheath Sealing Adapter, CPS SafeSheath Sealing Adapter, GE Healthcare PDF, 49KB, File does not meet accessibility standards Date: 16. June 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04848/10

Recall of SPOT-Light HER2 CISH Kit (Lot-No. 849398A), Life Technologies PDF, 592KB, File does not meet accessibility standards Date: 15. June 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01945/11

Problem with MLC and field size changes to XiO plans, Elekta CMS software PDF, 76KB, File is accessible Date: 15. June 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02896/10