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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

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

Safety issues on AW Server product, GE Healthcare PDF, 326KB, File does not meet accessibility standards Date: 22. December 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 05844/11

Lot recall of Lenscare SH-System Monatslinsen (monthly lens), 4CARE AG PDF, 457KB, File does not meet accessibility standards Date: 22. December 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 05552/11

Batch recall of Optiplug® Cement Restrictors, Integra LifeSciences PDF, 127KB, File does not meet accessibility standards Date: 22. December 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 05678/11

Lot recall for Vancomycin Calibrators (Lot-No. 59391741), ThermoFisher PDF, 48KB, File does not meet accessibility standards Date: 22. December 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 05588/11

Recall for Terumo Sarns Adult Rigid Intracardiac Suckers, Terumo Europe NV PDF, 50KB, File does not meet accessibility standards Date: 20. December 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04697/11

Recall of the device NL8600401 – Non-sterile stainless steel stepdown connector, Integra NeuroSciences PDF, 76KB, File does not meet accessibility standards Date: 16. December 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 05782/11

Safety Notice for the FrameArray Module (of the Optical Guidance Platform), Varian medical systems PDF, 384KB, File does not meet accessibility standards Date: 16. December 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 05698/11

Recall for AIA-PACK ß HCG Calibrator Set, TOSOH Bioscience PDF, 3MB, File does not meet accessibility standards Date: 16. December 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 05501/11

Safety Notice for 4D Structure Merge Tool Option in Eclipse Release 8.5-10 with 4D Planning, Varian medical systems PDF, 440KB, File does not meet accessibility standards Date: 16. December 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 05590/11

Lot Recall of 1 DAY ACUVUE MOIST contact lenses, Johnson & Johnson Vision Care PDF, 63KB, File does not meet accessibility standards Date: 15. December 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 05644/11

Safety Notice concerning Revolution XR/d X-ray Systems, GE Healthcare PDF, 30KB, File does not meet accessibility standards Date: 15. December 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 05605/11