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Corrective action for ACE Control, Trinity Biotech PDF, 91KB, File does not meet accessibility standards Date: 13. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00302/14

Corrective action for NCL-L-CD15 (Novocastra™ Liquid Mouse Monoclonal Antibody), Leica Biosystems PDF, 2MB, File does not meet accessibility standards Date: 12. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00247/14

Corrective action for Dimension Vista Enzyme 1 Calibrator, Siemens PDF, 23KB, File does not meet accessibility standards Date: 12. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00516/14

Safety Notice for the XGEO GC80, GC80V 80 und GC80V 65 X-ray systems, Samsung PDF, 187KB, File does not meet accessibility standards Date: 12. February 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 00008/14

Recall of the Select 3D™ and Select CAP™ Arterial Cannula product families, Medtronic PDF, 110KB, File does not meet accessibility standards Date: 11. February 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00417/14

Recall of the DYONICS 25 Patient Tube Set, Smith & Nephew PDF, 70KB, File does not meet accessibility standards Date: 11. February 2014 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 00514/14

Safety Notice for the ADEPT® Hip Resurfacing System (Finsbury Orthopaedics Ltd.), DePuy PDF, 79KB, File does not meet accessibility standards Date: 11. February 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00068/14

Recall for the Treatment Packs, Carl Zeiss Meditec AG PDF, 296KB, File does not meet accessibility standards Date: 10. February 2014 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 00496/14

Safety Notice for several Combi-Sets, containing BD™ Plastipak 50ml Luer Lok Syringes, Paul Hartmann AG PDF, 266KB, File does not meet accessibility standards Date: 10. February 2014 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - others
Reference 00442/14

Safety Notice for the Medtronic Mosaic™ Porcine Aortic Bioprosthesis, Medtronic Inc. PDF, 65KB, File does not meet accessibility standards Date: 10. February 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - cardiac surgery
Reference 00039/14

Safety Notice concerning the Puritan Bennett 840 ventilator and Puritan Bennett 700 series ventilators, Covidien PDF, 69KB, File does not meet accessibility standards Date: 10. February 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 00236/14

Recall for the blood products CompoStop and Compoflex, Fresenius Kabi PDF, 7MB, File does not meet accessibility standards Date: 10. February 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 07559/13

Corrective action for Immulite 2000 and Immulite 2000 XPi Osteocalcin, Siemens PDF, 22KB, File does not meet accessibility standards Date: 10. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00360/14

Corrective action for ACON On Call® Advanced Blood Glucose Monitoring System, ACON Laboatories PDF, 333KB, File does not meet accessibility standards Date: 07. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00337/14

Safety Corrective Action for the Hemofiltration Device AQUARIUS (regular platform 6), Nikkiso Deutschland GmbH PDF, 4MB, File does not meet accessibility standards Date: 07. February 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 00804/13

Recall of the product Low Profile Port with 6.6 Fr Single Lumen Broviac Catheter, Bard Access Systems Division PDF, 43KB, File does not meet accessibility standards Date: 07. February 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00159/14

Recall of the product AMO TECNIS iTec Preloaded Delivery System, Abbott Medical Optics Inc. PDF, 37KB, File does not meet accessibility standards Date: 07. February 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00169/14

Recall for the VA-LCP Distal Radius Plate, SYNTHES PDF, 947KB, File does not meet accessibility standards Date: 07. February 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00403/14

Safety Notice for the LOCATOR® Implant Attachment Systems, Zest Anchors LLC PDF, 88KB, File does not meet accessibility standards Date: 07. February 2014 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 00357/14

Recall of several articles and lots of the Anspach® Short Carbide Cutting Burrs, The Anspach Effort, Inc. PDF, 275KB, File does not meet accessibility standards Date: 06. February 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00297/14

Urgent Safety Notice for Camino® Advanced Monitors (CAM01), Integra NeuroSciences PDF, 131KB, File does not meet accessibility standards Date: 06. February 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 07520/13

Safety Notice concerning a corrective action of the defibrillator/pacer SLIM unit, part of the Corpuls3 system, GS Elektromedizinische Geräte G. Stemple GmbH PDF, 350KB, File does not meet accessibility standards Date: 06. February 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 00392/14

Corrective action for Cobas Integra 800 Software Version 9864.C2, Roche PDF, 84KB, File does not meet accessibility standards Date: 06. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05219/13

Follow up / Safety Notice for the LDD System, Calhoun Vision PDF, 123KB, File does not meet accessibility standards Date: 06. February 2014 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - other medical devices for ophthalmological purposes
Reference 07892/12

DePuy Synthes: recall of several Softlock forceps PDF, 2MB, File does not meet accessibility standards Date: 06. February 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 00301/14

Atrium Medical Cooperation: Recall of Atrium ATS drains PDF, 98KB, File does not meet accessibility standards Date: 06. February 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - drainages and suction systems
Reference 00268/14

Extended Recall for the XIA/XIA3/XIA Elegance/Mantis Redux Torque Wrenches, Stryker PDF, 2MB, File does not meet accessibility standards Date: 05. February 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05697/13

Recall of one lot of POWERFLEX® PRO PTA Dilatation Catheter, Cordis PDF, 299KB, File does not meet accessibility standards Date: 05. February 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07688/13

Recall for the product Competence Flow, Willmann & Pein PDF, 64KB, File does not meet accessibility standards Date: 05. February 2014 Topics: Medical devices Type: Customer information

Product group Dental products - dental material
Reference 00255/14

Safety Notice for the Peristeen Anal Irrigation System, Coloplast PDF, 123KB, File does not meet accessibility standards Date: 05. February 2014 Topics: Medical devices Type: Customer information

Product group Physical therapy - hydrotherapy
Reference 00096/14