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Safety Notice for the Femoral Segments - Endo-Model® SL® Rotational and Hinge Knee Prosthesis System, Waldemar Link GmbH & Co. KG PDF, 2MB, File does not meet accessibility standards Date: 09. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05277/12

Recall for MIRS Polyaxial Screw Body and MIRS Locking Cap, SYNTHES PDF, 444KB, File does not meet accessibility standards Date: 09. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05981/12

Safety Notice for the Centricity RIS-i system, GE Healthcare PDF, 33KB, File does not meet accessibility standards Date: 09. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 05873/12

Recall of further catalogue and batch numbers of the Cuticell Classic Paraffin Gauze, BSN medical GmbH PDF, 13KB, File does not meet accessibility standards Date: 09. October 2012 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - dressings
Reference 05354/12

Safety Notice for the Servoport 3000 m suction device, Servona GmbH PDF, 37KB, File does not meet accessibility standards Date: 09. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04549/12

Urgent Safety Notice for the Kryptonite bone cement, DOCTORS RESEARCH GROUP PDF, 40KB, File does not meet accessibility standards Date: 08. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - materials for implants
Reference 05988/12

Safety Notice concerning the Terumo® Advanced Perfusion System 1 - Central Control Monitor, Terumo CVS PDF, 90KB, File does not meet accessibility standards Date: 08. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05654/12

Safety Notice: Malfunction of the ABD Module or the Occluder Module for the Terumo® Advanced Perfusion System 1, Terumo CVS PDF, 81KB, File does not meet accessibility standards Date: 08. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05654/12

Safety Notice for the Terumo System 1 electronic patient gas system, Terumo CVS PDF, 102KB, File does not meet accessibility standards Date: 08. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05654/12

Safety Notice concerning various roller pump malfunctions of the Terumo® Advanced Perfusion System 1, Terumo CVS PDF, 92KB, File does not meet accessibility standards Date: 08. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05654/12

Safety Notice for the Clinac, Trilogy, Novalis Tx and Unique jaw carriers, Varian medical systems PDF, 358KB, File does not meet accessibility standards Date: 08. October 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 05987/12

Safety Notice for Dash 3000/4000/5000 patient monitor, GE Healthcare PDF, 44KB, File does not meet accessibility standards Date: 08. October 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 06232/12

Urgent Safety Notice: Recall of Aquavent Heated Ventilator and CPAP Breathing Circuits, Armstrong Medical Ltd. PDF, 90KB, File does not meet accessibility standards Date: 05. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05986/12

Safety Notice for the Sorin S5/C5 Perfusion System, Sorin Group PDF, 559KB, File does not meet accessibility standards Date: 04. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05818/12

Safety Notice for the Carestream DRX-Evolution X-ray system, Carestream Health PDF, 24KB, File does not meet accessibility standards Date: 04. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 03918/12

Safety Notice for the Axio Lab.A1 microscope, Carl Zeiss Microscopy GmbH PDF, 85KB, File does not meet accessibility standards Date: 04. October 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 06012/12

Lot Recall of BD Venflon Obturator 20GA, Becton Dickinson PDF, 43KB, File does not meet accessibility standards Date: 04. October 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 06131/12

Safety Notice for Agfa HealthCare IMPAX® Cardiovascular (IMPAX CV) products, Agfa HealthCare PDF, 50KB, File does not meet accessibility standards Date: 04. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 05888/12

Safety Notice for Washer / disinfector (endoscope disinfection unit), Steris PDF, 61KB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 05076/12

Urgent Safety Notice for the BIRMINGHAM HIP Modular Head, Smith & Nephew PDF, 63KB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06024/12

Safety Notice for Terumo® Advanced Perfusion System 1 / Network Power and communications, Terumo CVS PDF, 96KB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05654/12

Safety Notice for the air bubble detection system used with the Terumo® Advanced Perfusion System 1, Terumo CVS PDF, 91KB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05654/12

Safety Notice concerning the Sarns™ Centrifugal System for the Terumo® Advanced Perfusion System 1, Terumo CVS PDF, 79KB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05654/12

Safety Notice concerning Brilliance CT 6, 16, MX8000 v. EXP and Gemini Dual systems, Philips PDF, 132KB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 06035/12

Safety Notice concerning MX 16-Slice CT systems, Philips PDF, 1MB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 06104/12

Recall for the Spiralok Suture Anchors, DEPUY MITEK PDF, 39KB, File does not meet accessibility standards Date: 01. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05869/12

Safety Notice for VISALIS S500 and VISALIS V500, Carl Zeiss Meditec AG PDF, 84KB, File does not meet accessibility standards Date: 01. October 2012 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 04407/12

Urgent Product Recall for the PillCam® Express Delivery Devices, Given Imaging PDF, 41KB, File does not meet accessibility standards Date: 01. October 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 06064/12

Recall of the product Urgo Aphthen, Urgo GmbH PDF, 120KB, File does not meet accessibility standards Date: 01. October 2012 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - dressings
Reference 06095/12

Safety Notice concerning use of Oncentra MasterPlan and Oncentra External Beam, Nucletron PDF, 35KB, File does not meet accessibility standards Date: 01. October 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 05770/12