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Corrective action for BD FACS 7-Color Setup Beads, Becton Dickinson PDF, 61KB, File does not meet accessibility standards Date: 23. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00232/11

Safety Notice for Coulter® LH 750 and 780 Analyzer, Coulter® LH 500 Series System and Coulter® GEN S ™ System, Beckman Coulter PDF, 156KB, File does not meet accessibility standards Date: 23. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00605/11

Recall for Total Knee 2100, Össur PDF, 34KB, File does not meet accessibility standards Date: 23. March 2011 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 00687/11

Safety Notice for Brilliance 6, 10, 16, 16P, 40, 64, Big Bore, iCT and iCT SP, Philips PDF, 167KB, File does not meet accessibility standards Date: 23. March 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00590/11

Safety Notice for the device GE Centricity™ PACS-IW, GE Healthcare PDF, 39KB, File does not meet accessibility standards Date: 22. March 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04243/10

Safety Notice for UniCel DxC and Synchron LX Clinical Systems, Beckman Coulter PDF, 84KB, File does not meet accessibility standards Date: 22. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03917/10

Safety Notice for the SEVEN and SEVEN Plus Continuous Glucose Monitoring Systems, Dexcom Inc. PDF, 222KB, File does not meet accessibility standards Date: 22. March 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00406/11

Safety Notice for Carescape Monitor B850, GE Healthcare PDF, 48KB, File does not meet accessibility standards Date: 22. March 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01296/11

Safety Notice for the device GE Centricity™ PACS, GE Healthcare PDF, 40KB, File does not meet accessibility standards Date: 22. March 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04444/10

Corrective action and recall for the enGen Laboratory Automation System, Ortho PDF, 113KB, File does not meet accessibility standards Date: 22. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00450/11

Expanded Safety Notice for BrightSpeed Excel / Edge / Elite Select and BrightSpeed Elite CT Systems, GE Healthcare PDF, 157KB, File does not meet accessibility standards Date: 21. March 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00491/11

Safety Notice for BV Libra, BV Endura and BV Pulsera mobile X-ray systems, Philips PDF, 161KB, File does not meet accessibility standards Date: 21. March 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00563/11

Safety Notice for PACS Workstation IDS7 version 12.2.3., SECTRA PDF, 23KB, File does not meet accessibility standards Date: 21. March 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04731/10

Recall of Access Thyroglobulin Antibody II A32898 (Lot-No. 012741, 014751, 016551 and 016838), Beckman Coulter PDF, 33KB, File does not meet accessibility standards Date: 21. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00514/11

Recall of GEM Premier 4000 Glucose and Lactate Sensors due to falsely positive results, Instrumentation Laboratory PDF, 101KB, File does not meet accessibility standards Date: 21. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01188/11

Lot recall of DCI Dynamic Cervical Spine Implant, PARADIGM SPINE PDF, 67KB, File does not meet accessibility standards Date: 18. March 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01244/11

Recall of Alcohol pads and swabsticks, VWR International GmbH PDF, 1MB, File does not meet accessibility standards Date: 17. March 2011 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 00585/11

Recall of cobas c pack CA (Lot-No. 630204-01 and 631376-01), Roche PDF, 83KB, File does not meet accessibility standards Date: 17. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00927/11

Safety Notice for analysers of CS-2x00i series because of erroneous results due to heparin interference, Sysmex PDF, 22KB, File does not meet accessibility standards Date: 16. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00741/11

Lot recall of Drehmomentschlüssel 10NM M.T-Griff, model number NE160R, Aesculap AG PDF, 117KB, File does not meet accessibility standards Date: 16. March 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00658/11

Problem with backup unit of CARDIOHELP-i, the manually operated CARDIOHELP Emergency Drive (REF: 70104.8002), MAQUET Getinge Group PDF, 1MB, File does not meet accessibility standards Date: 16. March 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01059/11

Error in German Translation of Combitube Instruction for Use, Covidien PDF, 100KB, File does not meet accessibility standards Date: 15. March 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04777/10

Corrective action for ABL90 Flex, Radiometer PDF, 49KB, File does not meet accessibility standards Date: 14. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00247/11

Safety Notice for EEG recorder NicoletOne® System, CareFusion PDF, 104KB, File does not meet accessibility standards Date: 14. March 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02542/10

Safety Notice for the device Monaco, Elekta CMS Software PDF, 58KB, File does not meet accessibility standards Date: 14. March 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04654/10

Recall of Rhino Fiberscope Sheath, Medical Technical Promotion GmbH PDF, 221KB, File does not meet accessibility standards Date: 14. March 2011 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 00984/11

Safety Notice for the device XiO®, Elekta PDF, 112KB, File does not meet accessibility standards Date: 11. March 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02672/10

Lot Recall for Dermabond Skin Adhesive, Ethicon PDF, 273KB, File does not meet accessibility standards Date: 11. March 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00571/11

Recall for the DynaChip HLA Antibody Analysis System, Invitrogen PDF, 225KB, File does not meet accessibility standards Date: 11. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00485/11

Safety Notice for the device XiO®, Elekta PDF, 114KB, File does not meet accessibility standards Date: 11. March 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02699/10