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Recall for Human sTfR Quantikine IVD Elisa, R&D Systems PDF, 63KB, File does not meet accessibility standards Date: 27. April 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00851/09

Safety Information for Groove wheelchairs, Sunrise Medical PDF, 46KB, File does not meet accessibility standards Date: 27. April 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 04162/08

Corrective Action for VENTIlogic LS, Weinmann PDF, 98KB, File does not meet accessibility standards Date: 27. April 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00869/09

New Advisory Notice for Metha Hip Endoprothesis, Aesculap PDF, 160KB, File does not meet accessibility standards Date: 24. April 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03774/08

Safety Information for Flashlight PC-ECG, Medset PDF, 231KB, File does not meet accessibility standards Date: 24. April 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00907/09

Recall for Sekusept Extra N, ECOLAB PDF, 144KB, File does not meet accessibility standards Date: 24. April 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 00944/09

Recall for Dolomite Soprano rollator, Invacare PDF, 33KB, File does not meet accessibility standards Date: 24. April 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 00692/09

Information for Visage CS 3.1, Visage Imaging PDF, 36KB, File does not meet accessibility standards Date: 24. April 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00870/09

Recall Suture Material, Aesculap PDF, 92KB, File does not meet accessibility standards Date: 23. April 2009 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 00836/09

Recall for monitor component of the LifeVest system, Zoll Lifecor PDF, 31KB, File does not meet accessibility standards Date: 23. April 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00191/09

Recall for ProcedurePak, Mölnlycke Health Care PDF, 171KB, File does not meet accessibility standards Date: 22. April 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01083/09

Recall for Sirus Tibia Intramedullary Nail, Zimmer PDF, 77KB, File does not meet accessibility standards Date: 22. April 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01086/09

Recall for Op-Flex Poole, OP-set Poole, OP-handle Pool, Unomedical PDF, 347KB, File does not meet accessibility standards Date: 22. April 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01043/09

Recall for MRS-Cemented Stems, Stryker PDF, 82KB, File does not meet accessibility standards Date: 21. April 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00797/09

Recall for MarrowStim Kit, Biomet PDF, 131KB, File does not meet accessibility standards Date: 21. April 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00998/09

Safety Notice for Ovation MR Scanner, GE Healthcare PDF, 62KB, File does not meet accessibility standards Date: 21. April 2009 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 00862/09

Recall for Vitros Chemistry Products DT Calibrator Kit, Ortho Clinical Diagnostics PDF, 134KB, File does not meet accessibility standards Date: 21. April 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00651/09

Safety Notice and Software upgrade for model 8870 application card, Medtronic PDF, 226KB, File does not meet accessibility standards Date: 20. April 2009 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 00844/09

Safety Information for EP-4 Computerised Cardiac Stimulator, St. Jude Medical PDF, 101KB, File does not meet accessibility standards Date: 20. April 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00887/09

Safety Notice for CT Scanner Presto and ECLOS, Hitachi PDF, 54KB, File does not meet accessibility standards Date: 20. April 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00860/09

Recall for Ultrapro Mesh, Johnson & Johnson PDF, 76KB, File does not meet accessibility standards Date: 20. April 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01017/09

Recall for InterTan Entry Portal Handle, Smith and Nephew PDF, 56KB, File does not meet accessibility standards Date: 17. April 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00801/09

Recall for laparotomie set "Foliodrape CombiSet", Paul Hartmann PDF, 148KB, File does not meet accessibility standards Date: 16. April 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00983/09

Recall for Infinity™ Glucose Hexokinase Liquid Stable Reagent, Fisher Diagnostics PDF, 323KB, File does not meet accessibility standards Date: 16. April 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00921/09

Recall for Retroflex Introducer Sheath Set, Edwards Lifesciences PDF, 70KB, File does not meet accessibility standards Date: 16. April 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01021/09

Another Recall for Triathlon Primary Cemented Baseplate, Stryker PDF, 272KB, File does not meet accessibility standards Date: 16. April 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00269/09

Recall for Triathlon Primary Cemented Baseplate, Stryker PDF, 280KB, File does not meet accessibility standards Date: 16. April 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00234/09

Recall for ThromboType® plus-Kits, Hain Lifescience PDF, 50KB, File does not meet accessibility standards Date: 15. April 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00941/09

Recall for Wiseguide Guide Catheter, Boston Scientific PDF, 859KB, File does not meet accessibility standards Date: 15. April 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00945/09

Recall for Hydra „Blue“ Hydrophilic Coated Nitinol Guide Wire, OptiMed PDF, 170KB, File does not meet accessibility standards Date: 15. April 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00904/09