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Safety Notice for Mobile Monitoring Gateway (MMG) and Cardiomax, Ascom AB PDF, 102KB, File does not meet accessibility standards Date: 17. September 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 05061/12

Corrective action for the Previ Isola System, Biomerieux PDF, 58KB, File does not meet accessibility standards Date: 17. September 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 05849/12

Safety Notice for SureSigns VSi/VS2 Patient Monitors, Philips Healthcare PDF, 231KB, File does not meet accessibility standards Date: 17. September 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 05917/12

Safety Notice for the Bluephase G2 and Bluephase 20i Polymerisation Light, Ivoclar Vivadent AG PDF, 38KB, File does not meet accessibility standards Date: 14. September 2012 Topics: Medical devices Type: Customer information

Product group Dental products - equipment
Reference 04598/12

Safety Notice for LifeCare 4200 PCA Infusion System, Hospira Inc. PDF, 444KB, File does not meet accessibility standards Date: 14. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 05570/12

Safety Notice for the EkoSonic MACH4 Endovascular Device, EKOS Corporation PDF, 41KB, File does not meet accessibility standards Date: 14. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 05505/12

Safety Notice for Hemodraw® Closed Blood Sampling System, Smiths Medical PDF, 289KB, File does not meet accessibility standards Date: 14. September 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electronic blood pressure monitor
Reference 05041/12

Recall for the Terumo Syringe - 30ml Luer Lock/ Centric, Terumo Europe NV PDF, 334KB, File does not meet accessibility standards Date: 14. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 05835/12

Safety Notice for the superDimension systems with software version 4.0-4.9 PDF, 468KB, File does not meet accessibility standards Date: 14. September 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 04446/12

Safety Notice concerning the purification unit for medical air EcoPharm Tower, Dräger PDF, 289KB, File does not meet accessibility standards Date: 13. September 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05763/12

Safety Notice for Invasive Blood Pressure Cable, GE Healthcare PDF, 39KB, File does not meet accessibility standards Date: 13. September 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 05715/12

Recall of the Instrument Set for the Lubinus SPII Anatomically Adapted Hip Prosthesis System, Waldemar Link GmbH PDF, 180KB, File does not meet accessibility standards Date: 13. September 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04191/12, 04192/12, 04193/12

Recall of all lots for the DUET TRS Universal Straight und Articulating Single Use Loading Units, Covidien PDF, 1,012KB, File does not meet accessibility standards Date: 13. September 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 05544/12

Safety Notice for the product "Neue Ulmer Hüftorthese", Nea Tec PDF, 35KB, File does not meet accessibility standards Date: 12. September 2012 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - orthoses
Reference 04152/11

Recall for the Gliding Nail GN Blade Handle, Smith & Nephew Orthopaedics PDF, 49KB, File does not meet accessibility standards Date: 12. September 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05769/12

Safety Notice for the Chrystal LT 201 X-ray system from the manufacturer XCAN AG, MTS Maschinenbau AG PDF, 73KB, File does not meet accessibility standards Date: 12. September 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 04547/12

Lot Recall for the Twinplusdrain drainage catheter, Peter Pflugbeil GmbH PDF, 652KB, File does not meet accessibility standards Date: 12. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - drainages and suction systems
Reference 05722/12

Safety Notice concerning the FreeSpan™ Traverse and FreeSpan Ultra Twin™ Traverse, Liko AB PDF, 696KB, File does not meet accessibility standards Date: 11. September 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 04013/12

Safety Notice concerning the Flex Large 4 coil for Magnetom Skyra, Verio, Spectra and Biograph mMR systems PDF, 406KB, File does not meet accessibility standards Date: 11. September 2012 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 05718/12

Lot Recall for the “Achsstielknie” prosthesis, AQ Implants GmbH PDF, 58KB, File does not meet accessibility standards Date: 11. September 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05568/12

Safety Notice for the physical exercise Genius ECO body tension, Frei AG PDF, 217KB, File does not meet accessibility standards Date: 11. September 2012 Topics: Medical devices Type: Customer information

Product group Physical therapy - massage / mobility devices
Reference 01027/12

Korrekturmaßnahme für Control Unit TSM und Control Unit TSM 7900MT, Roche PDF, 52KB, File does not meet accessibility standards Date: 10. September 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05506/12

Corrective Action for Control Unit TSM and Control Unit TSM 7900MT, Roche PDF, 52KB, File does not meet accessibility standards Date: 10. September 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05506/12

Safety Notice concerning the Infant Ventilator Leoni Plus, Heinen + Löwenstein PDF, 63KB, File does not meet accessibility standards Date: 10. September 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05134/12

Safety Notice concerning the Minivator Bath Bliss bath lift 311, Handicare Ltd. PDF, 247KB, File does not meet accessibility standards Date: 10. September 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 05462/12

Corrective Action for ADVIA Centaur and ADVIA Centaur XP, Siemens PDF, 36KB, File does not meet accessibility standards Date: 10. September 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05601/12

Recall for Surgical Heart Valves, Edwards Lifesciences PDF, 55KB, File does not meet accessibility standards Date: 07. September 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - cardiac surgery
Reference 03504/12

Urgent Safety Notice for the AES Ankle prosthesis, Transystème PDF, 352KB, File does not meet accessibility standards Date: 07. September 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 04810/12

Recall for Sterrad 100S Cassette, ASP Advanced Sterilization Products PDF, 65KB, File does not meet accessibility standards Date: 07. September 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 04689/12

Lot Recall for AsidLine 75, Asid Bonz GmbH PDF, 12KB, File does not meet accessibility standards Date: 06. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion kits
Reference 05202/12