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Corrective action/Recall for Lab Vision Pretreatment Module, Thermo Fisher Scientific PDF, 131KB, File does not meet accessibility standards Date: 08. August 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02732/08

Information for Solar 8000M/i, GE Healthcare PDF, 184KB, File does not meet accessibility standards Date: 08. August 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02792/08

Recall for Mölnlycke ProcedurePaks®, Mölnlycke Health Care PDF, 129KB, File does not meet accessibility standards Date: 07. August 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02747/08

Recall for Universal-Set Landshut, Mölnlycke PDF, 121KB, File does not meet accessibility standards Date: 07. August 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02617/08

Recall for SYNCHRON Acetaminophen Reagent (ACTM), Beckman Coulter PDF, 93KB, File does not meet accessibility standards Date: 07. August 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02871/08

Information for Innova 3100 and 4100, GE Healthcare PDF, 49KB, File does not meet accessibility standards Date: 06. August 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02844/08

Recall for Vitesse Biopsy needle, OptiMed PDF, 120KB, File does not meet accessibility standards Date: 06. August 2008 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02884/08

Recall for Endoureterotomy Stent Set, Cook PDF, 88KB, File does not meet accessibility standards Date: 06. August 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02689/08

Recall for ECMO-Cannulae EKA 88 M, Maquet PDF, 62KB, File does not meet accessibility standards Date: 06. August 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02880/08

Information for BenchMark and Discovery Series, VENTANA PDF, 346KB, File does not meet accessibility standards Date: 05. August 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02776/08

Safety Notice for MOSAIQ and Multi-ACCESS, IMPAC PDF, 20KB, File does not meet accessibility standards Date: 05. August 2008 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02455/08

Information for Lifepak CR Plus defibrillator / Lifepak Express defibrillator, Medtronic PDF, 27KB, File does not meet accessibility standards Date: 05. August 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02870/08

Information for CASMED 740 Series Multiparameter Monitor, CASMED PDF, 148KB, File does not meet accessibility standards Date: 04. August 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02739/08

Information for MRI Magnet Venting System, Philips PDF, 25KB, File does not meet accessibility standards Date: 04. August 2008 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 02778/08

Safety Notice for Affinity Four Birthing Bed, Hill-Rom Inc. PDF, 295KB, File does not meet accessibility standards Date: 04. August 2008 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02636/08

Safety Notice for Axis and Irix Gamma Cameras, Philips PDF, 122KB, File does not meet accessibility standards Date: 04. August 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02504/08

Recall for Argyle™ Suction Catheter, Tyco Healthcare PDF, 168KB, File does not meet accessibility standards Date: 01. August 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02818/08

Recall for Reflex Revision Screwdriver, Stryker PDF, 137KB, File does not meet accessibility standards Date: 01. August 2008 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02163/08

Safety Notice for HeartMate II LVAS System Controller, Thoratec Corp. PDF, 88KB, File does not meet accessibility standards Date: 01. August 2008 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 00995/08

Information for Maximo II ICD/CRT-D, Medtronic PDF, 14KB, File does not meet accessibility standards Date: 31. July 2008 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02816/08

Recall for Thin-Flex Venous Return Cannulae, Edwards Lifesciences PDF, 81KB, File does not meet accessibility standards Date: 31. July 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02748/08

Information for Essenta DR, Philips PDF, 68KB, File does not meet accessibility standards Date: 31. July 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02259/08

Information for DICOMxchange, MeVis BreastCare PDF, 123KB, File does not meet accessibility standards Date: 30. July 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02736/08

Corrective Action/Recall for ARCHITECT AFP, Abbott PDF, 119KB, File does not meet accessibility standards Date: 30. July 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02614/08

Corrective action for Cobas b 221, Roche PDF, 111KB, File does not meet accessibility standards Date: 30. July 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02596/08

Recall for dual Lumen Catheter, Gyrus ACMI Inc. PDF, 133KB, File does not meet accessibility standards Date: 29. July 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02603/08

Recall for Portex Blue Line Ultra Tracheostomy Kit, Smiths Medical PDF, 165KB, File does not meet accessibility standards Date: 29. July 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02463/08

Recall for Portex® Blue Line Ultra Tracheostomy Kit, Smiths Medical PDF, 110KB, File does not meet accessibility standards Date: 28. July 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02594/08

Corrective action for Dimension Vista System, Siemens PDF, 33KB, File does not meet accessibility standards Date: 28. July 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02600/08

Corrective action/Recall for Galileo Instrument, IMMUCOR PDF, 156KB, File does not meet accessibility standards Date: 28. July 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02593/08