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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

Information concerning the X-ray systems Allura Xper FD20/10 and FD20 with Smart Mask option from Philips PDF, 38KB, File does not meet accessibility standards Date: 09. October 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02875/07

Recall of Architect Free T3 from Abbott Date: 08. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03475/07

Corrective action of ABL80 from Radiometer PDF, 38KB, File does not meet accessibility standards Date: 08. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01239/07

Corrective action for XE-Series Haematology Analyzers from Sysmex PDF, 30KB, File does not meet accessibility standards Date: 04. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03476/07

Recall of the Cord Clamp Clippers from Unomedical PDF, 74KB, File does not meet accessibility standards Date: 02. October 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01432/07

Information concerning a software discrepancy for use of MOSAIQ from Elekta Limited PDF, 110KB, File does not meet accessibility standards Date: 02. October 2007 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02811/07

Information concerning the HeartStart XL M4735A defibrillators from Philips Medizinsysteme Böblingen PDF, 47KB, File does not meet accessibility standards Date: 02. October 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02402/07

Corrective action of Varian High Energy and Low Energy Clinacs from Varian Medical Systems PDF, 175KB, File does not meet accessibility standards Date: 01. October 2007 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03423/07

Information about a temperature increase of the transducer surface from Toshiba Medical Systems PDF, 91KB, File does not meet accessibility standards Date: 28. September 2007 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 02497/07

Field safety notice concerning the KALIX II flat foot implant from Newdeal PDF, 234KB, File does not meet accessibility standards Date: 28. September 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02770/07

Recall of the HemoCue Glucose 201 RT System from HemoCue PDF, 59KB, File does not meet accessibility standards Date: 26. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03391/07

Corrective action and recall of the Dimension Clinical Chemistry System (software version 7.4SP1) from Dade Behring PDF, 76KB, File does not meet accessibility standards Date: 26. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03386/07

Recall of the Superflex ring strippers of the first generation from Fehling Instruments PDF, 36KB, File does not meet accessibility standards Date: 26. September 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02505/07