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Safety Notice concerning the STERRAD 200 System Carriages, ASP PDF, 141KB, File does not meet accessibility standards Date: 22. April 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 01558/13

Recall of the Constellation® Pneumatic Handpiece, DSP, Alcon PDF, 89KB, File does not meet accessibility standards Date: 22. April 2013 Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 02178/13

Safety Notice for Perfusor compact pumps, B. Braun Melsungen AG PDF, 28KB, File does not meet accessibility standards Date: 22. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01816/13

Additional Safety Notice for OEC Uroview X-ray systems, GE Healthcare PDF, 61KB, File does not meet accessibility standards Date: 22. April 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03227/06

Field Safety Notice for ExacTrac 5.x, Brainlab PDF, 645KB, File does not meet accessibility standards Date: 19. April 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 00837/13

Corrective action for Dimension Vista Systems, Siemens PDF, 161KB, File does not meet accessibility standards Date: 19. April 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 01697/13

Recall for CPD10 Cefpodoxime, Oxoid PDF, 22KB, File does not meet accessibility standards Date: 17. April 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 00922/13

Corrective Action for Vista Drug 4 Calibrator 4 (KC460) and Vista Drug 4 Calibrator 4 (KC460A), Siemens Healthcare PDF, 33KB, File does not meet accessibility standards Date: 17. April 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01112/13

Safety Notice for Gemstar Infusion System, Hospira Inc. PDF, 1MB, File does not meet accessibility standards Date: 17. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 01344/13

Safety Notice for the Acuson SC2000 ultrasound system, Siemens PDF, 2MB, File does not meet accessibility standards Date: 17. April 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 02085/13

Safety Notice for the Medsolutions4U Multi-Function Lifepak Electrodes, BIO-DETEK INCORPORATED PDF, 2MB, File does not meet accessibility standards Date: 16. April 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 01325/13

Recall for several NIM TriVantage EMG Endotracheal Tubes, Medtronic Xomed Inc. PDF, 32KB, File does not meet accessibility standards Date: 16. April 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 01329/13

Recall for NOR10 Norfloxacin, Oxoid PDF, 22KB, File does not meet accessibility standards Date: 16. April 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 01204/13

Recall of Thopaz Docking Stations, Medela AG PDF, 1MB, File does not meet accessibility standards Date: 16. April 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 00721/13

Safety Notice for Philips IntelliVue Information Center iX (PIIC iX), Philips Healthcare PDF, 433KB, File is accessible Date: 16. April 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 01618/13

Urgent Safety Notice for LIFEPAK CR® Plus and LIFEPAK EXPRESS® AEDs, Physio-Control PDF, 183KB, File does not meet accessibility standards Date: 15. April 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 01123/13

Safety Information for Hemofreeze bags, Fresenius PDF, 58KB, File does not meet accessibility standards Date: 15. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 00428/13

Lot Recall for the DHS/DCS Screw, SYNTHES PDF, 611KB, File does not meet accessibility standards Date: 15. April 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 01952/13

Urgent Safety Notice for the Penlon Sigma Delta Vaporizer, Penlon PDF, 315KB, File does not meet accessibility standards Date: 15. April 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 01886/13

Lot Recall for the Femoral Neck Screw Ø 11.0 mm, SYNTHES PDF, 572KB, File does not meet accessibility standards Date: 15. April 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 01502/13

Information about the safe handling of the Joline Acute Dialysis Catheters, Joline GmbH & Co KG PDF, 1MB, File does not meet accessibility standards Date: 15. April 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00970/13

Recall of specific Lot-Numbers of disposable laryngoscope battery handles, Teleflex PDF, 1MB, File does not meet accessibility standards Date: 15. April 2013 Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 02529/12

Safety Notice for the Tack-IT Endovascular Stapler®, Intact Vascular PDF, 97KB, File does not meet accessibility standards Date: 12. April 2013 Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 01403/13

Corrective action for AQURE Version 1.4.0 to 1.5.3, Radiometer PDF, 50KB, File does not meet accessibility standards Date: 12. April 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01196/13

Corrective Action for VITEK® 2 PCs, BioMérieux PDF, 223KB, File does not meet accessibility standards Date: 12. April 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 01068/13

Safety Notice for OEC Flexiview 8800 X-ray system, GE Healthcare PDF, 696KB, File does not meet accessibility standards Date: 12. April 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03227/06

Recall for OneTouch® Verio®IQ Blood Glucose Meters, Lifescan PDF, 43KB, File does not meet accessibility standards Date: 12. April 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01338/13

Recall for the Belly Bag® Urine Collection bag with Hip belt, Teleflex Medical PDF, 111KB, File does not meet accessibility standards Date: 12. April 2013 Type: Customer information

Product group Orthopaedic / Rehabilitation technology - care of natural and artificial body orifices
Reference 01699/13

Safety Notice for the NeuViz Dual and NeuViz 16 CT systems, Philips and Neusoft Medical PDF, 527KB, File does not meet accessibility standards Date: 11. April 2013 Type: Customer information

Product group Radiological technology - CT scanners
Reference 01133/13