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Extended Product Recall for Philips catheters AG55, Coloplast PDF, 94KB, File does not meet accessibility standards Date: 10. February 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04657/08

Safety Notice for AXIOM Artis systems regarding Quantification Software, Siemens PDF, 159KB, File does not meet accessibility standards Date: 10. February 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00113/09

Safety Notice for X-ray systems OEC 7600 and OEC 7700, GE Healthcare PDF, 66KB, File does not meet accessibility standards Date: 02. February 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00122/09

Urgent customer information of Pierre Fabre Dermo Cosmetique concerning Ducray Itax lotion 75 ml PDF, 1MB, File does not meet accessibility standards Date: 30. January 2009 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 00088/09

Recall of ConMed Endoscopic Disposable Polypectomy Snares and Gastrostomy Feeding Systems-EnTake™ PEG PDF, 167KB, File does not meet accessibility standards Date: 30. January 2009 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 04788/08

Safety Notice for Centricity PACS RA 1000 Workstation, GE Healthcare PDF, 83KB, File does not meet accessibility standards Date: 30. January 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04881/08

Recall for Genesis II Mobile Bearing Inlay, Smith & Nephew PDF, 117KB, File does not meet accessibility standards Date: 28. January 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04147/08

Information of Luer connector of specific A/V and S/N haemo­dialysis tubing systems for the 5008 PDF, 2MB, File does not meet accessibility standards Date: 28. January 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04497/08

Corrective action of Xcelens SA, Switzerland for Cartridge “IDEA cart” PDF, 4MB, File does not meet accessibility standards Date: 28. January 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 04669/08

Recall for Reflection hip, PE inlay, Smith & Nephew PDF, 58KB, File does not meet accessibility standards Date: 28. January 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04599/08

Safety Notification concerning a risk for the Injectomat TIVA Agilia syringe pump PDF, 504KB, File does not meet accessibility standards Date: 28. January 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04817/08

Safety Notice for Quatrix acrylic intraocular lens with a preloaded injector, Croma PDF, 5MB, File does not meet accessibility standards Date: 28. January 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00049/09

The company Intuitive Surgical notified customers of the da Vinci ® surgical system PDF, 323KB, File does not meet accessibility standards Date: 28. January 2009 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03178/07

Recall for Gold Probe™ Single-Use Bipolar Electrohemostasis Catheter, Boston Scientific PDF, 127KB, File does not meet accessibility standards Date: 28. January 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00005/09

Recall for TruCal Homocysteine FS, TruLab Homocysteine FS Level I and TruLab Homocysteine FS Level II, DiaSys PDF, 69KB, File does not meet accessibility standards Date: 26. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03167/08

Recall of Siemens Healthcare Diagnostics Diagnostics / NovaTec Immundiagnostica for Novagnost Release Kit Version 2008-08 PDF, 2MB, File does not meet accessibility standards Date: 26. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04449/08

Safety Notice for F1 Dental Chair, FIMET OY PDF, 70KB, File does not meet accessibility standards Date: 26. January 2009 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 00062/09

Safety Notice for ARTISTE with syngo RT Therapist Version 4.1 build 67, Siemens PDF, 92KB, File does not meet accessibility standards Date: 26. January 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04769/08

Field Safety Notice about a problem with the power supply for Terumo APS System 1 PDF, 1MB, File does not meet accessibility standards Date: 26. January 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01890/08

Recall of the spreader bars of the personal lift Invacare Flamingo PDF, 8MB, File does not meet accessibility standards Date: 26. January 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 00091/09

Field Safety Notice concerning increased leakage radiation from CT /e and HiSpeed X/I families of Computed Tomography systems PDF, 198KB, File does not meet accessibility standards Date: 26. January 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00006/09

Recall of the intraocluar lenses PC 430Y Eliteseries PDF, 556KB, File does not meet accessibility standards Date: 23. January 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04776/08

Field Safety Notice concerning digital Linear Accelerator Artiste PDF, 659KB, File does not meet accessibility standards Date: 23. January 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04771/08

Safety Notice for the patient lifts Liko Uno, Liko Light, Viking S and Viking XS, Liko AB PDF, 418KB, File does not meet accessibility standards Date: 23. January 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 00081/09

Recall of Siemens Healthcare Diagnostics Diagnostics (Thermofisher) for Dade Lipid Control Products PDF, 506KB, File does not meet accessibility standards Date: 21. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00018/09

Recall for IMMULITE 2000/2500 Digital Fluidics PC Board, Siemens PDF, 176KB, File does not meet accessibility standards Date: 20. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00013/09

Recall for HMRS Humerus Head Fixed and HMRS Distal Humerus Cone, STRYKER PDF, 68KB, File does not meet accessibility standards Date: 20. January 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03876/08

Recall for Ribbon Gauze with Vaseline 2cm x 10m and Clauden Wadding 5g, Lohmann & Rauscher PDF, 81KB, File does not meet accessibility standards Date: 20. January 2009 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 00016/09

Field Safety Notice concerning X-ray systems OrbixTop and ArcoSphere PDF, 728KB, File does not meet accessibility standards Date: 19. January 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04202/08