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Recall for the Compensator Slider Lambda 6x20, Carl Zeiss PDF, 96KB, File does not meet accessibility standards Date: 18. December 2013 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 07350/13

Safety Notice for the Leica M525 F50 / Leica M525 C50 Surgical Microscope with XY-Unit, Leica Microsystems PDF, 158KB, File does not meet accessibility standards Date: 18. December 2013 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 07204/13

Safety Notice for Targon FN plate and the Telescrews, AESCULAP PDF, 2MB, File does not meet accessibility standards Date: 18. December 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07254/13

Safety Notice for the use of sandblaster devices, 3M Espe PDF, 48KB, File does not meet accessibility standards Date: 18. December 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental material
Reference 01249/13

Safety Notice for Dräger monitor arm AC3000, Dräger PDF, 887KB, File does not meet accessibility standards Date: 18. December 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 06967/13

Corrective action for RealTime High Risk HPV and RealTime High Risk (HR) HPV m 2000 System ROW Combined Application CD-ROM, Abbott PDF, 792KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 06944/13

Software Upgrade for DigitalDiagnost X-ray systems with 3.0.x Software, Philips Medical Systems PDF, 115KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 07169/12

Recall for the Access Immunoassay Systems and Access hLH Calibrators, Beckman Coulter PDF, 37KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07142/12

Corrective Action for all Access/Access 2 Immunoassay-Systems, SYNCHRON LXi 725 Clinical-Systems and UniCel DxC 600i SYNCHRON Access Clinical-Systems, Beckman Coulter PDF, 39KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07118/12

Safety Notice concerning a corrective action of the Philips Invivo Expression MRI Patient Monitoring System, Philips Healthcare PDF, 69KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 07138/12

Recall of specific lots of the ExoSeal™Vascular Closure Device listed below, Cordis Corp. PDF, 203KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 06827/12

Corrective action for Coulter LH 750 and Coulter LH 780 Hematology Analyzer, Beckman Coulter PDF, 314KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 05937/13

Corrective action for the UniCel DxH 800 and 600 Coulter Cellular Analysis System, Beckman Coulter PDF, 538KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 07176/13

Safety Notice for Brivo OEC 715/785/865 C-Arm systems, GE Healthcare PDF, 52KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - mobile radiological diagnostic facilities
Reference 06209/13

Corrective action for Dxl 600 and Access 2, Beckman Coulter PDF, 89KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07168/13

Corrective Action for DELFIA/Auto / DELFIA Enhancement Solution, PerkinElmer PDF, 3MB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06331/13

Urgent Safety Information for the product Incor® Control Unit, Berlin Heart GmbH PDF, 796KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 07041/13

Corrective Action for LIAISON Control Mumps IgG, DiaSorin PDF, 1MB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 06266/13

Safety Notice for Artis systems running software version VC21B, Siemens Healthcare PDF, 2MB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 06725/13

Safety Notice for OsseoCare Pro iPad® app software release 1.2.0.7, Bien‐Air Dental PDF, 144KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Dental products - equipment
Reference 06396/13

Safety Notice for Brilliance CT Big Bore Oncology, Brilliance CT Big Bore Radiology and Brilliance CT 16 (Air) systems, Philips PDF, 178KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 05770/13

Corrective action for Vitros Immunodiagnostic Products CA 125 II Calibrators, Ortho PDF, 166KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 06142/13

Corrective action for Vitros Chemistry Products Na+ Slides und Vitros Chemistry Products Calibrator Kit 2, Ortho PDF, 264KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06355/13

Safety Notice for qLabs PT-INR Q-1 Pro Test Systems, nal von minden PDF, 619KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00466/13

Safety Notice for Vivid E9 4D ultrasound system, GE Healthcare PDF, 71KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 06624/13

Safety Notice for dental chair A-dec 200, A-dec PDF, 462KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 04663/13

Safety Notice for Elekta motorized wedges in RayStation 3.0, 3.5 and 4.0, RaySearch Laboratories PDF, 110KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 06352/13

Safety Notice concerning the Manual Film Composer Issue on Brivo CT315/325, Brivo CT385, Optima CT520 and Optima CT540, GE Healthcare PDF, 55KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 06534/13

Safety Notice for Discovery NM/CT670, Optima NM/CT640, Discovery NM630 and Brivo NM615, GE Healthcare PDF, 47KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 06399/13

Updated Safety Notice concerning the automated Blood Collection, Terumo PDF, 66KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 02797/13