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14,984 results

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Recall for UniCel DxI Immunoassay Systems, Beckman Coulter PDF, 552KB, File does not meet accessibility standards Date: 13. January 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05351/11

Safety Notice concerning Definium 8000 and Discovery XR650 systems, GE Healthcare PDF, 41KB, File does not meet accessibility standards Date: 13. January 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 05994/11

Lot Recall of the bone cement Palacos MV+G, HERAEUS PDF, 383KB, File does not meet accessibility standards Date: 12. January 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - materials for implants
Reference 05395/11

Corrective action for Accu Chek Aviva Plasma Import Test Strips, Servoprax PDF, 162KB, File does not meet accessibility standards Date: 12. January 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04416/11

Safety Notice concerning the Walker Etac ONO, Etac PDF, 146KB, File does not meet accessibility standards Date: 11. January 2012 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 05007/11

Corrective Action of MEE-1000A Neuromaster, Nihon Kohden PDF, 70KB, File does not meet accessibility standards Date: 06. January 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 05984/11

Safety Notice for AXIS and IRIX SPECT Systems, Philips PDF, 104KB, File does not meet accessibility standards Date: 05. January 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 05861/11

Recall of Sekisui Medical TPLA Calibrator Set and Sekisui Medical TPLA Control Set PDF, 80KB, File does not meet accessibility standards Date: 05. January 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 04457/11

Safety Notice for the Philips Ingenuity CT, Philips PDF, 115KB, File does not meet accessibility standards Date: 05. January 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 05927/11

Safety Notice for Senographe 2000D Mammography systems, GE Healthcare PDF, 45KB, File does not meet accessibility standards Date: 05. January 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for mammographic diagnostics
Reference 05906/11

Safety Notice for the Diagnost 94, 96 or 97 systems, Philips PDF, 398KB, File does not meet accessibility standards Date: 05. January 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 05917/11

Safety Notice for the device cobas c 311 analyzer, Roche Diagnostics GmbH PDF, 88KB, File does not meet accessibility standards Date: 03. January 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04749/11

Safety Notice for the product Accu-Chek Inform II, Roche PDF, 49KB, File does not meet accessibility standards Date: 03. January 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04973/11

Recall for the DA360 Knee system, Biomet PDF, 84KB, File does not meet accessibility standards Date: 03. January 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05543/11

Safety Information for the SUPER TORQUE® Angiographic Catheter with marker band, Cordis PDF, 35KB, File does not meet accessibility standards Date: 03. January 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 05609/11

Safety Information regarding different Celsite port systems, B.Braun Medical S.A.S. PDF, 144KB, File does not meet accessibility standards Date: 03. January 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 04269/11

Lot Recall for the Multifly needle, Sarstedt AG PDF, 92KB, File does not meet accessibility standards Date: 02. January 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 05663/11

FDA advice concerning Massager “ShoulderFlex” distributed by King International Date: 30. December 2011 Topics: Medical devices Type: Article

The US Food and Drug Administration (FDA) advises to stop using massager ShoulderFlex, distributed by King International (Beaverton, Oregon, USA).

Safety Information for the device CyberKnife Systems with the Lung Optimized Treatment Option, Accuray Inc. PDF, 1MB, File does not meet accessibility standards Date: 30. December 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 05740/11

Lot Recall for the Profemur® AM Stem Ti Plasma, Wright Medical Technology Inc. PDF, 852KB, File does not meet accessibility standards Date: 29. December 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 05982/11

Safety Notice/Recall for Mini Crosser M1, Mini Crosser A/S PDF, 27KB, File does not meet accessibility standards Date: 29. December 2011 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 05786/11

Safety Notice for Monosyn Violet 3/0 (2) 70 CM HR26 (M), Braun Surgical PDF, 213KB, File does not meet accessibility standards Date: 29. December 2011 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 02601/11

Recall of ACROBAT, ACROBAT V, ACROBAT SUV, XPOS 3 and XPOs 4, Maquet PDF, 748KB, File does not meet accessibility standards Date: 28. December 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 05767/11

Corrective action of surgical lighting systems iLED and TruLight, Trumpf Medizin Systeme GmbH & Co. KG PDF, 102KB, File does not meet accessibility standards Date: 23. December 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 05933/11

Field Safety Notice regarding power cords supplied with certain models of AIRVO PT100 and PT101 humidifiers, Fisher & Paykel PDF, 178KB, File does not meet accessibility standards Date: 23. December 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 05764/11

Problem with Optical Guidance Platform (OGP), Varian medical systems PDF, 188KB, File does not meet accessibility standards Date: 22. December 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03576/11

Field Safety Notice concerning a corrective action of the electrocardiogram (ECG) Screening software, Spacelabs Healthcare PDF, 115KB, File does not meet accessibility standards Date: 22. December 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 05363/11

Recall of several lots and adjustments sets of the contact lens AVAIRA Sphere, CooperVision Manufacturing Inc. PDF, 46KB, File does not meet accessibility standards Date: 22. December 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 05363/11

Absent wedge filter following plan load to Varian Treatment verify and record system, Varian medical systems PDF, 208KB, File does not meet accessibility standards Date: 22. December 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03909/10

Field safety corrective action on electrosurgical unit ESG-400, Olympus Winter & Ibe GmbH Date: 22. December 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 05769/11