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14,979 results

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Corrective Action for the Philips Ultrasound QLAB software, Philips Healthcare - Ultrasound PDF, 218KB, File does not meet accessibility standards Date: 29. December 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 08101/14

Corrective Action related to da Vinci Si System Vision Side Carts with threaded-in caster wheels, Intuitive Surgical PDF, 142KB, File does not meet accessibility standards Date: 29. December 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 08273/14

Corrective Action for the Trellis 8 Peripheral Infusion System, Covidien PDF, 103KB, File does not meet accessibility standards Date: 29. December 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 08422/14

Urgent Safety Notice for the Philips Model EPIQ 7 Ultrasound System, Philips Healthcare PDF, 188KB, File does not meet accessibility standards Date: 29. December 2014 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 08095/14

Corrective Action regarding Unomedical a/s infusion sets comfort™, comfort™ short and contact™ detach PDF, 177KB, File does not meet accessibility standards Date: 29. December 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 07800/14

Corrective Action for Humeral Broaches Aequalis, Tornier SAS PDF, 2MB, File does not meet accessibility standards Date: 29. December 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 08159/14

Urgent Safety Notice for the EndoBarrier® Gastrointestinal Liner with Delivery System, GI Dynamics, Inc. PDF, 195KB, File does not meet accessibility standards Date: 29. December 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 08211/14

Urgent Safety Notice for the Sensei® X Robotic Catheter System (Sensei X System), Hansen Medical, Inc. PDF, 145KB, File does not meet accessibility standards Date: 18. December 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - navigation systems
Reference 08134/14

Safety Notice for the MAGEC® Spinal Bracing and Distraction System, Ellipse Technologies, Inc. PDF, 178KB, File does not meet accessibility standards Date: 18. December 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05954/14

Recall for the Intraocular lenses (IOL) EUROMAXX ALI 313 and EUROMAXX A 313, ARGONOPTICS® GmbH & Co. KG PDF, 23KB, File does not meet accessibility standards Date: 18. December 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 08204/14

Recall for Autopen, Autopen 24, Densupen and Autopen 3 ml for Teriparatide, Owen Mumford Ltd. PDF, 458KB, File does not meet accessibility standards Date: 18. December 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - insulin pens and pen cannulas
Reference 08343/14

Corrective action for Brainlab iPlan RT / iPlan RT Dose radiation treatment planning software, Brainlab AG PDF, 327KB, File does not meet accessibility standards Date: 18. December 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 08129/14

Corrective action for the Curved Reinforced Endotracheal Tubes and other devices for tracheal intubation, Teleflex Medical PDF, 152KB, File does not meet accessibility standards Date: 17. December 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 08126/14

Corrective action for Siemens Digital Linear Accelerators of type MEVATRON™, PRIMUS™, ONCOR™ and ARTISTE™, Siemens AG
PDF, 16KB, File does not meet accessibility standards
Date: 17. December 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 07844/14

Corrective action for Artis Q ceiling Systems, Siemens AG Healthcare PDF, 3MB, File does not meet accessibility standards Date: 17. December 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 08125/14

Safety Notice for the Philips HeartStart MRx Monitor/Defibrillator, Philips Healthcare PDF, 76KB, File does not meet accessibility standards Date: 17. December 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 08100/14

Safety Information concerning frisbee cervical disc prosthesis, ulrich GmbH & Co. KG PDF, 20KB, File does not meet accessibility standards Date: 17. December 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07775/14

Corrective action for the MAS® CardioImmune XL Level 1 Control, Microgenics GmbH /Thermo Fisher Scientific PDF, 3MB, File does not meet accessibility standards Date: 17. December 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06912/14

Corrective action for Dimension Vista® Myoglobin Calibrator (MYO CAL), Siemens Healthcare Diagnostics Inc. PDF, 24KB, File does not meet accessibility standards Date: 16. December 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07932/14

Urgent Safety Notice for the ID cards "NaCl, Enzyme Test and Cold Agglutinins", DiaMed GmbH PDF, 2MB, File does not meet accessibility standards Date: 16. December 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06634/14

Corrective action for the Phadia 1000 instrument, Phadia AB PDF, 153KB, File does not meet accessibility standards Date: 16. December 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 08022/14

Corrective action for the product LIAISON® Borrelia IgG, DiaSorin S.p.A. PDF, 655KB, File does not meet accessibility standards Date: 16. December 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 07768/14

Urgent Safety Notice for the Breas Vivo 50 Home Care Ventilator, Breas Medical AB PDF, 91KB, File does not meet accessibility standards Date: 16. December 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07942/14

Recall for the DePuy Synthes Trauma RIA (Reamer/Irrigator/Aspirator) System, Synthes GmbH PDF, 3MB, File does not meet accessibility standards Date: 16. December 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 08229/14

Updated Instruction for Use for Laparoscopic Manual Instruments and Accessories, Stryker Endoscopy PDF, 49KB, File does not meet accessibility standards Date: 16. December 2014 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 08177/14

Urgent Safety Notice/Update for the Brilliance CT series and other CT systems, Philips Healthcare PDF, 291KB, File does not meet accessibility standards Date: 15. December 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 02362/14

Corrective action for the ZOLL Pro-padz Sterile Multi-Function Electrodes, ZOLL Medical Corporation PDF, 2MB, File does not meet accessibility standards Date: 15. December 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 07823/14

Corrective action for the Philips HeartStart MRx Monitor/Defibrillator, Philips Healthcare PDF, 66KB, File does not meet accessibility standards Date: 15. December 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 08092/14

Corrective action for the product AlignRT, Vision RT PDF, 497KB, File does not meet accessibility standards Date: 15. December 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 07853/14

Recall for the Setpack® Toptex® lite Laparotomy Swab, green, Lohmann & Rauscher GmbH & Co. KG PDF, 44KB, File does not meet accessibility standards Date: 15. December 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07970/14