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Recall for Precision Xtra Plus Blood Glucose Test Strips, Abbott PDF, 58KB, File does not meet accessibility standards Date: 13. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02221/09

Safety Notice for MultiDiagnost Eleva with FD, Philips PDF, 91KB, File does not meet accessibility standards Date: 13. July 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02348/09

Safety Notice for Membrane Blue Syringes, DORC PDF, 75KB, File does not meet accessibility standards Date: 13. July 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00730/09

Safety Notice for Signa MR 3 T systems, GE Healthcare PDF, 64KB, File does not meet accessibility standards Date: 10. July 2009 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 02090/09

Safety Notice for Signa MR Excite 1.5T systems, GE Healthcare PDF, 68KB, File does not meet accessibility standards Date: 10. July 2009 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 02277/09

Recall for Ambix Intraport CP, Fresenius Kabi PDF, 107KB, File does not meet accessibility standards Date: 10. July 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02235/09

Corrective action for ACCU-Chek Performa Test Strips, Roche PDF, 78KB, File does not meet accessibility standards Date: 10. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02159/09

Recall for Endoloop Ligature PDS II Suture, Johnson & Johnson PDF, 84KB, File does not meet accessibility standards Date: 10. July 2009 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02093/09

Recall for Drain Feed PTCD Catheter, Peter Pflugbeil GmbH PDF, 76KB, File does not meet accessibility standards Date: 10. July 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01648/09

Safety Notice for NX software with CMS option, Agfa HealthCare PDF, 118KB, File does not meet accessibility standards Date: 09. July 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02275/09

Recall for angioplastie sets containing a hemostatic Y connector, Smiths Medical PDF, 138KB, File does not meet accessibility standards Date: 09. July 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02020/09

Safety Notice for Clinacs with C Series version 7.x, Varian PDF, 545KB, File does not meet accessibility standards Date: 09. July 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04118/08

Recall for Pump Hoses XD 2020, Ulrich medical PDF, 76KB, File does not meet accessibility standards Date: 09. July 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01430/09

Recall for Intro-Flex Percutaneous Sheath Introducer, Edwards Liefesciences Services PDF, 72KB, File does not meet accessibility standards Date: 08. July 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00474/09

Second Recall for Fem-Flex II Femoral Access Cannulae, Edwards Lifesciences PDF, 82KB, File does not meet accessibility standards Date: 08. July 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00150/09

Safety Notice for HiRes 90k Implant Magnet, Advanced Bionics PDF, 42KB, File does not meet accessibility standards Date: 08. July 2009 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02267/09

Safety Notice for CT Perfusion 4, GE Healthcare PDF, 130KB, File does not meet accessibility standards Date: 08. July 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02104/09

Safety Notice for Medos Oxygenators PDF, 30KB, File does not meet accessibility standards Date: 08. July 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01725/09

Recall for Posey Waist and Wrist Restraints PDF, 173KB, File does not meet accessibility standards Date: 07. July 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01958/09

Recall for GEHC 1.5 m and 1.8 m Uni-Circuit anesthesia breathing circuits, GE Healthcare PDF, 106KB, File does not meet accessibility standards Date: 07. July 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02096/09

Safety Notice for GE Signa OpenSpeed and Ovation MR Scanner, GE Healthcare PDF, 47KB, File does not meet accessibility standards Date: 07. July 2009 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 02021/09

Field Safety Notice of the Amplatzer® Cardiac Plug PDF, 57KB, File does not meet accessibility standards Date: 03. July 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01846/09

Recall of all “Action 2000” manual wheelchairs of manufacturer Invacare Aquatec GmbH PDF, 519KB, File does not meet accessibility standards Date: 02. July 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 00689/09

Recall of Powersail Coronary Dilation Catheters PDF, 39KB, File does not meet accessibility standards Date: 02. July 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02142/09

Recall of the hip belt supplied with the products Mobile Advance Seat, Contoured Advanced Seat, Squiggles Early Sitting System and Squiggles Saddle Seat PDF, 625KB, File does not meet accessibility standards Date: 01. July 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01185/09

Recall of actuators for care beds Casa Med II, Casa Vario T and Casa Comfort II PDF, 64KB, File does not meet accessibility standards Date: 01. July 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01933/09

Lot-recall regarding Sorbit-MacConkey-Agar with MUG PDF, 332KB, File does not meet accessibility standards Date: 01. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02105/09

Recall Fogarty occlusion catheters, Edwards Lifesciences PDF, 284KB, File does not meet accessibility standards Date: 30. June 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00425/09

Information about iron (rust) contamination of DI Water in ADVIA® LabCell® System Tubing, Siemens Healthcare Diagnostics PDF, 26KB, File does not meet accessibility standards Date: 30. June 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01940/09

Notice of Correction concerning Triage® TOX Drug Screen kits, Biosite Incorporated PDF, 143KB, File does not meet accessibility standards Date: 29. June 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01967/09