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Safety Notice concerning the implantable infusion pump Lenus pro, Tricumed Medizintechnik GmbH PDF, 3MB, File does not meet accessibility standards Date: 09. January 2014 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - drug pumps
Reference 07124/13

Safety Notice for Bedside Monitors series „Life Scope J“ BSM-9101K using software version 13-05, Nihon Kohden PDF, 118KB, File does not meet accessibility standards Date: 09. January 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 07902/13

Safety Notice for the product GALILEI G6 Lens Professional, Ziemer Ophthalmic Systems AG PDF, 197KB, File does not meet accessibility standards Date: 07. January 2014 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological diagnostics
Reference 07557/13

Recall for the Spare Elbow Kits, Fisher & Paykel PDF, 391KB, File does not meet accessibility standards Date: 07. January 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07921/13

Corrective action for the enteral feeding pump Amika, Fresenius Kabi PDF, 29KB, File does not meet accessibility standards Date: 06. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 07418/13

Additional Safety Notice for the Interventional Wires and Attain Hybrid® Guidewires, Medtronic PDF, 94KB, File does not meet accessibility standards Date: 06. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 06285/13

Lot Recall of the Presfit cup TiCP vitamys system, Mathys PDF, 172KB, File does not meet accessibility standards Date: 03. January 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07521/13

Updated Important Safety Notice for the Apex™ collimator, Elekta PDF, 277KB, File does not meet accessibility standards Date: 03. January 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 00420/13

Recall of two lots of the Axxess Drug Eluting Coronary Bifurcation Stent System, BIOSENSORS Europe SA PDF, 2MB, File does not meet accessibility standards Date: 03. January 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 07508/13

Recall for certain Split Cath III dialysis catheters, Medcomp Medical Components Inc. PDF, 2MB, File does not meet accessibility standards Date: 02. January 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07667/13

Important Information for the AMPLATZER™ Septal Occluder, St. Jude PDF, 128KB, File does not meet accessibility standards Date: 02. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 04657/12

Corrective action for Nova StatStrip and StatSensor Blood Monitoring Systems, Nova Biomedical PDF, 229KB, File does not meet accessibility standards Date: 02. January 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06565/13

Recall of one batch of the product AT LISA 809MP, Carl Zeiss Meditec AG PDF, 56KB, File does not meet accessibility standards Date: 02. January 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 07143/13

Safety Notice for sterEOS workstation, EOS imaging PDF, 2MB, File does not meet accessibility standards Date: 02. January 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 07249/13

Safety Notice for mobile X-Ray systems (Optima XR220amx, Optima XR200amx with Digital Upgrade), GE Healthcare PDF, 65KB, File does not meet accessibility standards Date: 30. December 2013 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 07421/13

Safety Notice for GEMINI TF 16, 64, Big Bore, TruFlight Select, GEMINI TF Ready and GEMINI LXL PET/CT systems, Philips PDF, 192KB, File does not meet accessibility standards Date: 30. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 07669/13

Recall for the ADEPT® Hip Resurfacing System, MatOrtho Ltd. PDF, 32KB, File does not meet accessibility standards Date: 23. December 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07125/13

Corrective action for Human IgM Kit for use on SPA PLUS, Binding Site PDF, 272KB, File does not meet accessibility standards Date: 23. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 06553/13

Lot Recall for the Tezo Titanium Cage, ULRICH GmbH & Co. KG PDF, 16KB, File does not meet accessibility standards Date: 23. December 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06463/13

Recall for “Laparascopic Instruments” due to a reprocessing issue, Rudolf Medical PDF, 77KB, File does not meet accessibility standards Date: 23. December 2013 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 07113/13

Recall of one batch of the Biolox Delta Trinity Modular Heads 36 mm, Corin PDF, 1MB, File does not meet accessibility standards Date: 23. December 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07416/13

Safety Information for all care beds manufactured 2010-2011, FMB Care GmbH PDF, 32KB, File does not meet accessibility standards Date: 23. December 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 03952/13

Urgent Safety Notice regarding implantable HeartWare LVAS, HeartWare Inc. PDF, 145KB, File does not meet accessibility standards Date: 23. December 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 07555/13

Safety Notice concerning the 550 TxT™ Treatment Table type PRIMUS™, ONCOR™ and ARTISTE™, Siemens Healthcare PDF, 120KB, File does not meet accessibility standards Date: 20. December 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 07434/13

Safety Notice concerning SOMATOM CT, Siemens Healthcare PDF, 120KB, File does not meet accessibility standards Date: 20. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 07570/13

Safety Notice STERRAD® 50, 100S, and 200 systems, ASP PDF, 31KB, File does not meet accessibility standards Date: 20. December 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 06945/13

Corrective action for the Fully Automated Blood Coagulation Analyzer, Sysmex PDF, 1MB, File does not meet accessibility standards Date: 18. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 06643/13

Corrective action of BioMerieux for ZYM B, API Listeria, API NH PDF, 117KB, File does not meet accessibility standards Date: 18. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 06901/13

Safety Notice for the ClinActiv® Therapy Surface, Hill-Rom PDF, 617KB, File does not meet accessibility standards Date: 18. December 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 05650/13

Safety Notice for the CoreValve™ AccuTrak™ Delivery Catheter System, Medtronic PDF, 78KB, File does not meet accessibility standards Date: 18. December 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07150/13