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Lot Recall for Super Arrow-Flex® Percutaneous Sheath Introducer Set with Integral Hemostasis Valve / Side Port, Teleflex Medical PDF, 180KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04748/10

Lot Recall for Amplatzer Sizing Balloon II, AGA Medical Corp. PDF, 103KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04792/10

Safety Notice for MAGNETOM Systems, Siemens Healthcare PDF, 60KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 03891/10

Corrective Action/Recall for Sensors for Seronorm Trace Elements Serum Level 2, SERO PDF, 46KB, File does not meet accessibility standards Date: 07. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03327/10

Lot Recall for FMS Intermediary Tube Sets for Fluid Management, DePuy Mitek PDF, 237KB, File does not meet accessibility standards Date: 07. January 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04675/10

Safety Notice for Spectra Optia Apheresis System, CaridianBCT PDF, 87KB, File does not meet accessibility standards Date: 07. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04637/10

Safety Notice for Licox CMP Tissue Oxygen Monitors, Integra LifeSciences PDF, 73KB, File does not meet accessibility standards Date: 07. January 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04778/10

Important Information for Potassium liquirapid, HUMAN PDF, 77KB, File does not meet accessibility standards Date: 06. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04434/10

Safety Notice for the Footswitch of the Allura FD10, FD20, CV20 systems and the Allura field extension series, Philips PDF, 168KB, File does not meet accessibility standards Date: 06. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04484/10

Safety Notice for GE Centricity PACS Web Diagnostic Software-Version 3.7.3, GE Healthcare PDF, 72KB, File does not meet accessibility standards Date: 06. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00228/10

Safety Notice for GE Centricity PACS Web Diagnostic Software, GE Healthcare PDF, 69KB, File does not meet accessibility standards Date: 06. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00228/10

Safety Notice for Presice Cryoablation Systems and SeedNet MRI Cryoablation Systems, GALILMedical PDF, 305KB, File does not meet accessibility standards Date: 05. January 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04580/10

Safety Notice for Centricity™ PACS RA1000 Workstation Software Versions 2.1x und 3.0x, GE Healthcare PDF, 679KB, File does not meet accessibility standards Date: 05. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00360/10

Safety Notice for Centricity™ PACS RA1000 Workstation Software, GE Healthcare PDF, 569KB, File does not meet accessibility standards Date: 05. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00360/10

Corrective Action/Recall for SYNCHRON Systems Glucose (GLU) Cartridge Reagent for use on UniCel and SYNCHRON Systems, Beckman Coulter PDF, 138KB, File does not meet accessibility standards Date: 05. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04462/10

Safety Notice for Riata and Riata ST silicone insulated defibrillation leads, St. Jude Medical PDF, 190KB, File does not meet accessibility standards Date: 04. January 2011 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 04703/10

Safety Information for the TDP® Gou Gong® lamp, T & K GmbH PDF, 44KB, File does not meet accessibility standards Date: 30. December 2010 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 03954/10

Recall for the swivel shower chair model Ben, Drive Medical GmbH & Co. KG PDF, 90KB, File does not meet accessibility standards Date: 30. December 2010 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 04635/10

Safety Notice for Access® Immunoassay Systems SHBG, Beckman Coulter PDF, 49KB, File does not meet accessibility standards Date: 30. December 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02989/10

Safety Notice for all GE Healthcare MR systems, GE-Medical Systems PDF, 62KB, File does not meet accessibility standards Date: 30. December 2010 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 04658/10

Safety Notice for Brainlab iPlan RT Dose Radiotherapy Treatment Planning Software, Brainlab PDF, 73KB, File does not meet accessibility standards Date: 29. December 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04353/10

Safety Notice for all CyberKnife Treatment Planning Systems, Accuray PDF, 42KB, File does not meet accessibility standards Date: 29. December 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04534/10

Expansion of the Recall for Immunglobulin A (Ig-A) Reagent, Beckman Coulter PDF, 57KB, File does not meet accessibility standards Date: 29. December 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02468/10

Urgent Safety Notice for counterfeit Nellcor SpO2 Durasensors, PDF, 270KB, File does not meet accessibility standards Date: 29. December 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04705/10

Recall for Zenith Branch Endovascular Graft Iliac Bifurcation, Cook PDF, 19KB, File does not meet accessibility standards Date: 29. December 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04699/10

Recall for the Great Ormond Street GOS Tracheostomy Cannula Set, Teleflex Medical PDF, 189KB, File does not meet accessibility standards Date: 28. December 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04706/10

Corrective Action/Recall for MIKRO 120 centrifuge, Andreas Hettich GmbH & Co. KG PDF, 104KB, File does not meet accessibility standards Date: 28. December 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01318/10

Safety Notice for PRIMEDIC™ AkuPak, Metrax GmbH PDF, 52KB, File does not meet accessibility standards Date: 28. December 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04399/10

Recall for DHEA RIA Kit, Beckman Coulter PDF, 79KB, File does not meet accessibility standards Date: 28. December 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04648/10