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Recall for Stryker Navigation PC SPC-1 system, Stryker Navigation – Stryker Leibinger PDF, 112KB, File does not meet accessibility standards Date: 03. December 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04048/09

Lot-Recall for SKY fast & fixed abutment 0°, BREDENT MEDICAL PDF, 37KB, File does not meet accessibility standards Date: 03. December 2009 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 04142/09

Safety Notice for MD-JADE 2 Software, MeVis Medical Solutions PDF, 104KB, File does not meet accessibility standards Date: 02. December 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04235/09

Recall for Biotrak Mini Drill and Long Cannulated Drill, Acumed PDF, 58KB, File does not meet accessibility standards Date: 02. December 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 04401/09

Safety Notice for Innova 2121IQ and 3131IQ cardiovascular X-ray systems, GE Healthcare PDF, 73KB, File does not meet accessibility standards Date: 02. December 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04267/09

Lot-Recall for Ziraldent Dental Implants, METOXIT PDF, 95KB, File does not meet accessibility standards Date: 01. December 2009 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 04106/09

Lot Recall for Intertan Hex Screw, Smith & Nephew PDF, 59KB, File does not meet accessibility standards Date: 30. November 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03961/09

Corrective Action for Bar Code Scanner, Abbott PDF, 58KB, File does not meet accessibility standards Date: 30. November 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04281/09

Recall for Oximetry-PODs model 7600B. Nonin PDF, 15KB, File does not meet accessibility standards Date: 30. November 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04255/09

Safety Notice for Kodak DirectView DR 9500, Carestream Health PDF, 80KB, File does not meet accessibility standards Date: 30. November 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04214/09

Lot Recall for NexGen Femoral Component, Zimmer PDF, 338KB, File does not meet accessibility standards Date: 30. November 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04294/09

Safety Notice for Enteral Nutrition Pump APPLIX Smart/Vision, Fresenius Kabi PDF, 28KB, File does not meet accessibility standards Date: 27. November 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04202/09

Corrective Action for Running UniCel Dxl System Software versions 4.2 or 4.2.1, Beckman Coulter PDF, 311KB, File does not meet accessibility standards Date: 27. November 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04273/09

Recall for Dimension Vista System Flex reagent cartridges, Siemens PDF, 97KB, File does not meet accessibility standards Date: 27. November 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04046/09

Recall for Advantage®, 2-Button Turbo Handpiece, ConMed Linvatec PDF, 183KB, File does not meet accessibility standards Date: 26. November 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04065/09

Recall for Cepheid LightCycler HSV ½ Qual Kit, Roche PDF, 27KB, File does not meet accessibility standards Date: 26. November 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03830/09

Safety Information for Respironics V60 ventilators, Philips PDF, 91KB, File does not meet accessibility standards Date: 26. November 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03922/09

Recall for Anti-Co(b), Immucor PDF, 124KB, File does not meet accessibility standards Date: 26. November 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04288/09

Recall for INNEX tibia inserts FIXSC, Zimmer PDF, 86KB, File does not meet accessibility standards Date: 26. November 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03846/09

Recall for KyphX HV-R Bone Cement, Elmdown Ltd. PDF, 176KB, File does not meet accessibility standards Date: 25. November 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04218/09

Recall for Protégé® EverFlex Biliary Stent System, Ev3 PDF, 67KB, File does not meet accessibility standards Date: 25. November 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04244/09

Urgent Information about the safe use of a dialysis tube set, B. Braun PDF, 260KB, File does not meet accessibility standards Date: 20. November 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04161/09

Recall for Morcellator Cutting Tubes, Richard Wolf GmbH PDF, 117KB, File does not meet accessibility standards Date: 20. November 2009 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03967/09

Information for RapidPoint 400 and 405 Systems, Siemens PDF, 30KB, File does not meet accessibility standards Date: 20. November 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04091/09

Recall for Tecnis™ 1-Piece IOL, AMO PDF, 154KB, File does not meet accessibility standards Date: 19. November 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04153/09

Corrective Action for VIDAS TPSA, Biomerieux PDF, 55KB, File does not meet accessibility standards Date: 19. November 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03920/09

Safety Notice for T-Piece Resuscitation Circuits, GE Healthcare PDF, 978KB, File does not meet accessibility standards Date: 19. November 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04030/09

Upgrading of the Corrective Action for α2-Macroglobulin-Reagent (AMG), Beckman Coulter PDF, 64KB, File does not meet accessibility standards Date: 19. November 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00613/08

Recall for BD Q-Syte and MPS Acacia with BD Q-Syte, Becton Dickinson PDF, 119KB, File does not meet accessibility standards Date: 18. November 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03978/09

Information for Exafit stems, Zimmer PDF, 137KB, File does not meet accessibility standards Date: 17. November 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04116/09