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Recall of Liaison CEA (lot number 72101) from DiaSorin PDF, 38KB, File does not meet accessibility standards Date: 29. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03667/07

Corrective action and recall for BD Multiset Software (versions 2.1, 2.11 and 2.2) from Becton Dickinson PDF, 133KB, File does not meet accessibility standards Date: 29. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03453/07

Recall of the Boots brand blood glucometers from Boots Date: 26. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03671/07

Recall of the locking Screws from Stryker PDF, 66KB, File does not meet accessibility standards Date: 25. October 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03349/07

Recall of the Frazier & Poole Suction instruments from ConMed PDF, 85KB, File does not meet accessibility standards Date: 25. October 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03463/07

Recall of the femoral cannulae from Sorin Group PDF, 124KB, File does not meet accessibility standards Date: 23. October 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03462/07

Recall of the ELS - cannulae from Maquet PDF, 75KB, File does not meet accessibility standards Date: 23. October 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03521/07

Information concerning the Corpuls 3 defibrillator from GS Elektromedizinische Geräte PDF, 544KB, File does not meet accessibility standards Date: 22. October 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03122/07

Information concerning the Spectra Optia apheresis system from Gambro PDF, 176KB, File does not meet accessibility standards Date: 22. October 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03331/07

Information concerning the RTP-Exchange v6.2, v6.6 & v8.0 from Varian PDF, 83KB, File does not meet accessibility standards Date: 19. October 2007 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03674/07

Information concerning the Tracheostomy Tube Holders 240 Blue and 242 Blue from DALE Medical Products PDF, 193KB, File does not meet accessibility standards Date: 19. October 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03458/07

Recall of the Airox ventilator systems Supportair, Smartair ST, Smartair Plus and Legendair from Tyco Healthcare PDF, 49KB, File does not meet accessibility standards Date: 19. October 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03342/07

Recall of the CAST 2000 Elisa (lot number 4421.1) from Bühlmann PDF, 38KB, File does not meet accessibility standards Date: 18. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03619/07

Corrective action for the Access Immunoassay Systems Ultrasensitive Insulin Reagent Kit from Beckman Coulter PDF, 37KB, File does not meet accessibility standards Date: 18. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03665/07

Recall of the transfer sets manufactured by Whatman which are shipped with Berinin P, Beriplex P/N, Beriate P, Haemate P or Humate-P from CSL Behring PDF, 96KB, File does not meet accessibility standards Date: 17. October 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02824/07

Recall of the Columbia blood agar with CNA from Heipha PDF, 33KB, File does not meet accessibility standards Date: 17. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03651/07

Information about incorrect display of Pulsed Wave Doppler velosity values on reloaded images from GE Healthcare PDF, 111KB, File does not meet accessibility standards Date: 16. October 2007 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 03591/07

Recall of one lot of the Transend EX™ Standard .014-Guidewires from Boston Scientific PDF, 142KB, File does not meet accessibility standards Date: 16. October 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03576/07

Recommendations for patients concerning the Sprint Fidelis leads from Medtronic PDF, 379KB, File does not meet accessibility standards Date: 16. October 2007 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03656/07

Recall of the hydrophobic acrylic intraocular lens Hydromax from Carl Zeiss Meditec PDF, 120KB, File does not meet accessibility standards Date: 16. October 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03161/07

Information concerning the OBI versions 1.2 and 1.3 with CBCT from Varian PDF, 205KB, File does not meet accessibility standards Date: 16. October 2007 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03507/07

Recall of the Vasofix cannulae 1,1 x 33 mm, 20G from B. Braun PDF, 56KB, File does not meet accessibility standards Date: 15. October 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03441/07

Corrective Action of the programmer software for Reply SR single chamber pacemakers from Sorin PDF, 89KB, File does not meet accessibility standards Date: 12. October 2007 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03232/07

Corrective action for the Swing Twin Sampler II from Diamed PDF, 35KB, File does not meet accessibility standards Date: 11. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02817/07

Safety notice concerning the OEC 9900, OEC 9800 and OEC 8800 X-ray systems from GE Healthcare PDF, 46KB, File does not meet accessibility standards Date: 09. October 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03095/07

Information concerning the OEC Miniview 6800 systems from GE Healthcare PDF, 33KB, File does not meet accessibility standards Date: 09. October 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03094/07

Information concerning the X-ray systems Allura Xper FD20/10 and FD20 with Xper-CT option from Philips PDF, 32KB, File does not meet accessibility standards Date: 09. October 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02875/07