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Corrective action for G8 Hemoglobin F&A2 Calibrator and Hemoglobin F and A2 Control, TOSOH Bioscience PDF, 160KB, File does not meet accessibility standards Date: 26. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04109/11

Recall for MKONA-Z and MKONA-1, Privates Institut für Immunologie und Molekulargenetik PDF, 288KB, File does not meet accessibility standards Date: 26. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04262/11

Safety Notice for several sets intended to be used with infusion pumps, Unomedical A/S PDF, 743KB, File does not meet accessibility standards Date: 23. September 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03931/10

Lot Recall of AVAIRA Toric contact lenses, CooperVision PDF, 837KB, File does not meet accessibility standards Date: 23. September 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 03948/11

Safety Notice for Synchromed II Implantable Drug Infusion Pumps, Medtronic PDF, 46KB, File does not meet accessibility standards Date: 23. September 2011 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 04254/11

Recall of all Pleura Flow Catheter Systems of the manufacturer Xeridiem Medical Devices, Clear Catheter Systems PDF, 41KB, File does not meet accessibility standards Date: 23. September 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01852/11

Recall for the Endoplege Coronary Sinus Catheter Kit, Edwards Lifesciences PDF, 65KB, File does not meet accessibility standards Date: 22. September 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02863/11

Corrective action for Advia 120/2120/2120i Hematology Systems, Siemens PDF, 29KB, File does not meet accessibility standards Date: 22. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04334/11

Recall for Clinical Chemistry Alkaline Phosphatase, Abbott PDF, 80KB, File does not meet accessibility standards Date: 21. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04033/11

Safety Notice for the Biolox® OPTION Ceramic Femoral Head System, Zimmer PDF, 355KB, File does not meet accessibility standards Date: 21. September 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04304/11

Safety Notice concerning use of Mizuho OSI Modular Table Systems, MIZUHOSI PDF, 244KB, File does not meet accessibility standards Date: 21. September 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03647/11

Safety Notice for the RT Chart function of ARIA, Varian medical systems PDF, 165KB, File does not meet accessibility standards Date: 19. September 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04084/11

Safety Notice for Advantage Workstation with Functool Option, GE Healthcare PDF, 44KB, File does not meet accessibility standards Date: 19. September 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04246/11

Recall for intrauterine probes (tubes) with lot numbers up to and including lot J13, Varian medical systems PDF, 58KB, File does not meet accessibility standards Date: 19. September 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04279/11

Urgent Safety Notice for the Mammomat Inspiration with Stereo Biopsy device, Siemens Healthcare PDF, 560KB, File does not meet accessibility standards Date: 19. September 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04015/11

Urgent Safety Notice concerning AVEA ventilators, CareFusion PDF, 49KB, File does not meet accessibility standards Date: 19. September 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04236/11

Safety Information for the Cemover device, Tecres S.p.A. PDF, 43KB, File does not meet accessibility standards Date: 19. September 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 04243/11

Safety Notice regarding Dash 3000/4000/5000 monitors, GE Healthcare PDF, 68KB, File does not meet accessibility standards Date: 19. September 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04244/11

Recall of Siemens for Dimension Vista CA19-9 Flex reagent cartridges PDF, 86KB, File does not meet accessibility standards Date: 16. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04020/11

Safety Notice for Varian High-Energy Clinac® linear accelerator, Varian medical systems PDF, 177KB, File does not meet accessibility standards Date: 16. September 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04163/11

Recall for Dimension EXL LOCI Cardiac Troponin I reagent cartridges, Siemens PDF, 34KB, File does not meet accessibility standards Date: 15. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04162/11

Recall for Dimension EXL LOCI Cardiac Troponin I, Siemens PDF, 35KB, File does not meet accessibility standards Date: 15. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04160/11

Recall for AU5800 Clinical Chemistry Analyzer, Beckman Coulter PDF, 32KB, File does not meet accessibility standards Date: 15. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03380/11

Safety Notice for the Magnus Hybrid operating table, Maquet Getinge Group PDF, 716KB, File does not meet accessibility standards Date: 15. September 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04048/11

Recall for the OXOID Egg Yolk Emulsion, Oxoid PDF, 164KB, File does not meet accessibility standards Date: 15. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03667/11

Recall for BD Vacutainer 2.7 ml Plus Citrate Blood Collection Tube, Becton Dickinson PDF, 37KB, File does not meet accessibility standards Date: 14. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02862/11

Recall for Anti-Cw micro, Immucor PDF, 24KB, File does not meet accessibility standards Date: 14. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04032/11

Corrective action for AQT90 FLEX TnI and TnT assays in connection with AQT90 FLEX βhCG assay due to a carry-over, Radiometer PDF, 33KB, File does not meet accessibility standards Date: 13. September 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03898/11