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Corrective action for Magna Pure 96 Instruments, Roche PDF, 108KB, File does not meet accessibility standards Date: 26. March 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01119/14

Urgent Safety Notice for "ViaCath" diagnostic catheters, VascoMed PDF, 130KB, File does not meet accessibility standards Date: 26. March 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01145/14

Recall of several lots of Osseofix Implants, Alphatec Spine PDF, 86KB, File does not meet accessibility standards Date: 26. March 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 01453/14

Safety Notice concerning a mispositioning of source, Eckert & Ziegler BEBIG GmbH PDF, 2MB, File does not meet accessibility standards Date: 26. March 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - nuclear medical therapeutic equipment
Reference 01464/14

Safety Notice for Propaq LT / Propaq 802 Models 802LTAN, 802LT0N, 802LTRN, Welch Allyn PDF, 43KB, File does not meet accessibility standards Date: 25. March 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 06576/13

Safety Notice for the C-SVV system, Chronos Vision GmbH PDF, 392KB, File does not meet accessibility standards Date: 25. March 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - ENT equipment
Reference 01169/14

Recall of the CUSA® Excel/CUSA® Excel+ 23 kHz Sterile Torque Wrench, Integra LifeSciences Services PDF, 111KB, File does not meet accessibility standards Date: 25. March 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 01297/14

Recall of several lots of RHK Femoral Components, Biomet PDF, 167KB, File does not meet accessibility standards Date: 25. March 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00692/14

Safety Notice for the device Standard Offset Cup Impactor, Greatbatch Medical PDF, 211KB, File does not meet accessibility standards Date: 25. March 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00694/14

Recall of several lots of AGC DA 2000 Femoral Components, Biomet PDF, 163KB, File does not meet accessibility standards Date: 25. March 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00639/14

Corrective action for actim CRP dipsticks, Medix Biochemica PDF, 226KB, File does not meet accessibility standards Date: 24. March 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00863/14

Recall of one lot of the cardiovascular shunt Coroflex Blue Neo, B. Braun PDF, 840KB, File does not meet accessibility standards Date: 24. March 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 01373/14

Recall of the "Laser beam guide, standard, single-use" and "Ophthalmic fiberoptic light instrument, single-use", Synergetics PDF, 3MB, File does not meet accessibility standards Date: 24. March 2014 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - laser technology
Reference 00182/14

Urgent Safety Notice for the Philips HeartStart MRx Monitor/Defibrillator, Philips Medical Systems PDF, 163KB, File does not meet accessibility standards Date: 24. March 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 01057/14

Important Information for the Ovation Prime™ Abdominal Stent Graft System, TriVascular PDF, 147KB, File does not meet accessibility standards Date: 24. March 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00967/14

Safety Notice concerning reprocessing of EndoWrist instruments, Intuitive Surgical Inc. PDF, 147KB, File does not meet accessibility standards Date: 24. March 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03954/11

Safety Notice for the device Plegiox Cardioplegia Heat Exchanger, MAQUET Cardiopulmonary AG PDF, 297KB, File does not meet accessibility standards Date: 24. March 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 00314/14

Corrective action of the samaritan PAD 500P public access defibrillators, HeartSine Technologies PDF, 188KB, File does not meet accessibility standards Date: 24. March 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 00916/14

Fresenius Kabi: Safety Notice for the blood bag systems COMPOFLOW, COMPOSTOP, COMPOFLEX and COMPOSELECT PDF, 376KB, File does not meet accessibility standards Date: 24. March 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 01179/14

Recall of one lot of the product Biomedics 1 day toric contact lenses, CooperVision PDF, 110KB, File does not meet accessibility standards Date: 21. March 2014 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - contact lenses
Reference 01516/14

Smiths Medical Deutschland: Safety Notice for Medex Custom Packs containing BD Plastipak 50 ml Luer Lok Syringes PDF, 358KB, File does not meet accessibility standards Date: 21. March 2014 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - others
Reference 00889/14

Safety Notice for the Kimal Procedure Packs containing Needle 18G x 7cm Sing Wall Cordis A4, Kimal Plc PDF, 106KB, File does not meet accessibility standards Date: 21. March 2014 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - others
Reference 01523/14

Safety Notice for Symbia T and Symbia T2 camera systems, Siemens PDF, 524KB, File does not meet accessibility standards Date: 21. March 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 01500/14

Safety Notice for the ExacTrac 6.0 Patient Positioning System, Brainlab AG PDF, 331KB, File does not meet accessibility standards Date: 20. March 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 00997/14

Corrective action for Freestyle Lite test strips, axicorp Pharma GmbH PDF, 6MB, File does not meet accessibility standards Date: 20. March 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00229/14

Recall of all Otto Bock Aerial and Aerial Active Wheelchair Cushions, Otto Bock PDF, 84KB, File does not meet accessibility standards Date: 20. March 2014 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - mobility aids
Reference 00435/14

Recall of the scissor blades 4393040 ModuBlade “Metzenbaum”, Richard Wolf GmbH PDF, 1MB, File does not meet accessibility standards Date: 20. March 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 01335/14

Urgent Safety Notice for ALTRUS® Thermal Tissue Fusion Handpieces, ConMed PDF, 30KB, File does not meet accessibility standards Date: 19. March 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 00953/14

Urgent Safety Notice for the device Alaris® SmartSite® Needle-Free Valve, CareFusion PDF, 65KB, File does not meet accessibility standards Date: 19. March 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion kits
Reference 01349/14

Important Safety Notice for latex breathing bags, Dräger PDF, 8MB, File does not meet accessibility standards Date: 19. March 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 01319/14