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Recall for HA Hip Stem, Stryker PDF, 23KB, File does not meet accessibility standards Date: 13. February 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00009/09

Recall for Omnican Pen 31, B. Braun PDF, 52KB, File does not meet accessibility standards Date: 13. February 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04784/08

Safety Notice for TEE/8-3 Transducer, SonoSite PDF, 22KB, File does not meet accessibility standards Date: 13. February 2009 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 03679/08

Recall for Aquaflow Collagen Glaucoma Drainage, Staar Surgical PDF, 87KB, File does not meet accessibility standards Date: 13. February 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04423/08

Safety Notice for Blizzard active wheelchair, Otto Bock PDF, 81KB, File does not meet accessibility standards Date: 12. February 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 04268/08

Safety Notice for AXIOM Artis and Artis zee, Siemens PDF, 237KB, File does not meet accessibility standards Date: 12. February 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00112/09

Recall for Oral Fluid Positive Control, Oral Fluid Negative Control and Oral Fluid Cutoff Calibrator, OraSure Technologies PDF, 233KB, File does not meet accessibility standards Date: 12. February 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03992/08

Safety Notice for Philips iSite PACS 4.1, Philips Healthcare PDF, 196KB, File does not meet accessibility standards Date: 12. February 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00182/09

Softwareupgrade für TEE/8-3 MHz Sonde am M-Turbo Ultraschallsystem, SonoSite PDF, 23KB, File does not meet accessibility standards Date: 11. February 2009 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 03679/08

Recall for Expanding polyvinyl alcohol (PVA) sinus tampons, SPIGGLE & THEIS PDF, 84KB, File does not meet accessibility standards Date: 11. February 2009 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 00134/09

Information for Bioball Metal Heads, Merete PDF, 50KB, File does not meet accessibility standards Date: 11. February 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04595/08

Corrective action for Medumat Transport, Weinmann Geräte für Medizin PDF, 70KB, File does not meet accessibility standards Date: 11. February 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04502/08

Safety Notice for Alaris GP Volumetric Pumps and Alaris GP Guardrails Volumetric Pumps, Cardinal Health PDF, 36KB, File does not meet accessibility standards Date: 10. February 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00007/09

Recall for ERAGON and POWERGRIP Forceps, Richard Wolf GmbH PDF, 56KB, File does not meet accessibility standards Date: 10. February 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04338/08

Safety Notice for Kehr/VanKemmel T-Drainage, Coloplast PDF, 61KB, File does not meet accessibility standards Date: 10. February 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04632/08

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