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Corrective action for the Zeus Infinity Empowered (IE) anaesthesia workstation with integrated patient monitoring, Dräger Medical GmbH PDF, 3MB, File does not meet accessibility standards Date: 30. May 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03064/14

Safety Information for the Infusion pump CODAN ARGUS 717/718V, control software version 5.05, Codan Argus AG PDF, 3MB, File does not meet accessibility standards Date: 30. May 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 02618/14

Updated Instructions for Use for Thermablate Endometrial Ablation System (EAS), Idoman Teoranta PDF, 576KB, File does not meet accessibility standards Date: 30. May 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02520/14

Corrective action for the MACROLYTE® Premie Dispersive Electrode, ConMed Corporation PDF, 107KB, File does not meet accessibility standards Date: 30. May 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02649/14

Corrective action for the IntelliVue Patient Monitors MP2, X2, MP5/MP5T and MP20-50 containing battery operation, Philips Healthcare PDF, 92KB, File does not meet accessibility standards Date: 30. May 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 02445/14

Corrective action for the Kryo range of freezers, Planer plc PDF, 384KB, File does not meet accessibility standards Date: 28. May 2014 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 02246/14

Corrective action for the "ReNew Fenestrated Grasper Forceps Tips", Microline Surgical PDF, 1MB, File does not meet accessibility standards Date: 28. May 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 03027/14

Recall for the MGuard Prime Coronary Stent System Embolic Protective Stent (EPS), InspireMD Ltd. PDF, 125KB, File does not meet accessibility standards Date: 28. May 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 02469/14

Corrective action for the Progressa™ Bed Mattress, Hill-Rom PDF, 9MB, File does not meet accessibility standards Date: 28. May 2014 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 02389/14

Corrective action for the DOA SALIVA MULTI-6 TEST, DIALAB GmbH PDF, 90KB, File does not meet accessibility standards Date: 28. May 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02291/14

Corrective action for the products Bondek and Tevdek, Teleflex Medical PDF, 195KB, File does not meet accessibility standards Date: 28. May 2014 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 03014/14

Recall for AMO TECNIS® CL Foldable Silicone IOL with OptiEdge Design, AMO Ireland PDF, 152KB, File does not meet accessibility standards Date: 28. May 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 02868/14

Safety Notice for the STIMPOD NMS450 Nerve Stimulator, Xavant Technology PDF, 261KB, File does not meet accessibility standards Date: 27. May 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 01873/14

Recall for the Medtronic Navigation Sterile Devices, Medtronic PDF, 231KB, File does not meet accessibility standards Date: 27. May 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02822/14

Important Safety Information concerning Valvuloplasty Catheters of type VACS II and VACS III, Osypka AG PDF, 161KB, File does not meet accessibility standards Date: 27. May 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - transfusion kits
Reference 01153/14

Recall of specific lots of Renma PTA Dilatation Catheters, ClearStream Technologies Ltd. PDF, 385KB, File does not meet accessibility standards Date: 27. May 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01638/14

Corrective action for the PROFEMOR® Modular Neck Extraction Plug - long and short, MicroPort Orthopedics PDF, 124KB, File does not meet accessibility standards Date: 27. May 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02112/14

Corrective action for Biolox Delta Ceramic Head 36mm Standard, Biomet UK Ltd. PDF, 1MB, File does not meet accessibility standards Date: 26. May 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 02407/14

Safety Notice for the MODULAR ANALYTICS <E 170>, MODULAR ANALYTICS EVO <E 170>, cobas e 601 module and cobas e 602 module, Roche Diagnostics PDF, 106KB, File does not meet accessibility standards Date: 26. May 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 02142/14

Recall for the Solar 8000M/i Patient Monitor, GE Healthcare PDF, 86KB, File does not meet accessibility standards Date: 26. May 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 02644/14

Recall for the GIS-10 OxyBloc Bite Block Device, Diagmed Healthcare Ltd. PDF, 238KB, File does not meet accessibility standards Date: 26. May 2014 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 02478/14

Urgent Safety Notic for the FreeStyle® Blood Glucose Monitoring System, Abbott Diabetes Care PDF, 904KB, File does not meet accessibility standards Date: 26. May 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00777/14

Additional Information for IMMULITE®/IMMULITE® 1000 and IMMULITE® 2000/IMMULITE® 2000 XPi Androstenedione assays, Siemens PDF, 33KB, File does not meet accessibility standards Date: 23. May 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00022/14

Safety Notice for the PARACHUTE Delivery System, CardioKinetix Inc. PDF, 43KB, File does not meet accessibility standards Date: 23. May 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 02601/14

Corrective action for the Calcium Gen.2 assay, Roche Diagnostics GmbH PDF, 117KB, File does not meet accessibility standards Date: 23. May 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01911/14

Urgent Safety Notice for the Kenex suspension arm with radiation shield and/or surgical lamp, GE Healthcare PDF, 79KB, File does not meet accessibility standards Date: 23. May 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 02595/14

Corrective action for the ARCHITECT EBV VCA IgM Controls, ABBOTT PDF, 21KB, File does not meet accessibility standards Date: 23. May 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 02697/14

Urgent Safety Notice concerning GE Warmers with Nellcor SpO2, GE Healthcare PDF, 165KB, File does not meet accessibility standards Date: 23. May 2014 Topics: Medical devices Type: Customer information

Product group Physical therapy - climatotherapy
Reference 02496/14