BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Search i

Search help

  • Enter one or more search terms in the search field. Upper and lower case are not relevant.
  • As soon as you have entered three letters in the search field, various search words will be suggested from which you can choose one.
  • If you are searching for a certain group of words, put these words in double quotes. The hits will then contain the words in the order you entered, e.g. "medicines for children".
  • Multiple search terms can also be combined with the Boolean operators AND and OR. When using the operator AND, the results contain the intersection of all search terms. When using the operator OR, the hits contain one of the search terms or only individual search terms. The result set is therefore significantly larger. Please note that these operators must be written in capital letters.
  • If you receive a (too) large number of hits as a result of your search, you can narrow it down by using filters. These filter options appear to the left of the search results and are subdivided into:

    • category (e.g. safety of medicinal products, medical devices, code systems)
    • format (e.g. download, risk information, DHPCs)
    • time interval (e.g. last 30 days, older than ...)
  • Selected filters can be removed individually or all at once ("Show all results").
  • By default, search results are sorted by relevance, but they can also be sorted chronologically ("Latest entries first" or "Oldest entries first").

Enter search term

14,982 results

Results per page: 10 20 30

Recall for NovaSure Radiofrequency Control Unit, Hologic Inc. PDF, 130KB, File does not meet accessibility standards Date: 17. February 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 00620/14

Lot Recall of the Cortex Screw, Synthes PDF, 2MB, File does not meet accessibility standards Date: 14. February 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00580/14

Corrective action for Advia 1800 und Advia 2400 ISE Firmware V2.23, Siemens PDF, 19KB, File does not meet accessibility standards Date: 14. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00399/14

Recall of the 200ml ELS Syringe for contrast media injector, Medtron AG PDF, 36KB, File does not meet accessibility standards Date: 14. February 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 00352/14

Safety Notice for the CT System SCENARIA / ECLOS, Hitachi PDF, 137KB, File does not meet accessibility standards Date: 14. February 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 00460/14

Urgent Safety Notice on PTA Balloon Dilatation Catheter product families (Models Coyote™ Over-The-Wire and Coyote™ Monorail™), Boston Scientific International PDF, 146KB, File does not meet accessibility standards Date: 14. February 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00615/14

Corrective action for XN-Series analysers, Siemens PDF, 58KB, File does not meet accessibility standards Date: 14. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 06148/13

Safety Notice for the product syngo Dynamics with Sensis integration licence, Siemens Healthcare PDF, 2MB, File does not meet accessibility standards Date: 14. February 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 00208/14

Safety Notice for Carescape Monitor B850 F5-01 Frame, GE Healthcare Finland Oy PDF, 72KB, File does not meet accessibility standards Date: 14. February 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 00486/14

Urgent Recall of one lot of the product “Emser Inhalationslösung 20er”, Siemens & CO PDF, 80KB, File does not meet accessibility standards Date: 14. February 2014 Topics: Medical devices Type: Customer information

Product group Physical therapy - inhalation therapy
Reference 00647/14

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