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Corrective action for Phosphorus Reagent, Abbott PDF, 24KB, File does not meet accessibility standards Date: 27. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04819/13

Corrective action for LIAISON® Control Direct Renin, Diasorin PDF, 575KB, File does not meet accessibility standards Date: 26. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04236/13

Corrective action for AQT 90 FLEX Analyzers, Radiometer PDF, 28KB, File does not meet accessibility standards Date: 26. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03940/13

Safety Notice for the Alphafit proximally modified stem, Corin Medical Ltd. PDF, 3MB, File does not meet accessibility standards Date: 26. August 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 03250/13

Safety Notice for the FUJIFILM Gastroscope EG-530UT2, FUJIFILM PDF, 69KB, File does not meet accessibility standards Date: 26. August 2013 Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 04900/13

Urgent Safety Notice concerning the TRACOE twist tracheostomy tube, Tracoe Medical GmbH PDF, 5MB, File does not meet accessibility standards Date: 26. August 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 04142/13

Lot recall of Scotchcast Wet or Dry Cast Padding, 3M Medica PDF, 28KB, File does not meet accessibility standards Date: 23. August 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - dressings
Reference 04773/13

Safety notice regarding HydroSet Injectable HA Bone Substitute, STRYKER PDF, 183KB, File does not meet accessibility standards Date: 22. August 2013 Type: Customer information

Product group Non-active implants - materials for implants
Reference 04404/13

Corrective action for Dimension Vista Systems RF Flex Reagent Cartridges, Siemens PDF, 54KB, File does not meet accessibility standards Date: 22. August 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 04135/13

Recall for Polarizers, Carl Zeiss PDF, 80KB, File does not meet accessibility standards Date: 21. August 2013 Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 02878/13

Information concerning change of expiration date, Johnson & Johnson PDF, 65KB, File does not meet accessibility standards Date: 21. August 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 04294/13

Lot recall of cardiotomy / autotransfusion reservoirs, Maquet Cardiopulmonary AG PDF, 33KB, File does not meet accessibility standards Date: 21. August 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - transfusion kits
Reference 01503/13

Lot recall of Expandable Introducer Sheath Set, Edwards Lifesciences PDF, 38KB, File does not meet accessibility standards Date: 21. August 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01101/13

Corrective action for Calcium CPC FS, Diasys PDF, 52KB, File does not meet accessibility standards Date: 20. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04842/13

Lot recall of dialysis blood tubing system, B.Braun Avitum AG PDF, 48KB, File does not meet accessibility standards Date: 20. August 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 02107/13

Corrective action for HLA Fusion-Software due to conversion error, One Lambda PDF, 404KB, File does not meet accessibility standards Date: 19. August 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 04782/13

Potential issue on a secondary touch screen, MAQUET PDF, 150KB, File does not meet accessibility standards Date: 19. August 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 04593/13

Safety Notice for the Dräger anesthesia machines Fabius GS Premium, Fabius OS, Fabius Plus and Fabius Tiro PDF, 22KB, File does not meet accessibility standards Date: 14. August 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 04707/13

Corrective action for Advia® 120 Hematology systems, Siemens PDF, 123KB, File does not meet accessibility standards Date: 14. August 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 03794/13

Lot Recall of the Trabecular Metal Reverse Glenosphere Helmet, Zimmer PDF, 285KB, File does not meet accessibility standards Date: 14. August 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04557/13

Corrective action for Advia Chemistry Systems A1c_3 Calibrator, Siemens PDF, 89KB, File does not meet accessibility standards Date: 14. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04596/13

Recall for Suture Anchors of the Bioraptor, Osteoraptor and Twinfix Ultra product line, SMITH & NEPHEW PDF, 74KB, File does not meet accessibility standards Date: 14. August 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 04655/13

Lot Recall of VKMO 30000 (Quadrox -i Pediatric + VHK 31000), Maquet Cardiopulmonary AG PDF, 413KB, File does not meet accessibility standards Date: 14. August 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02533/13

Corrective action for Dimension Vista 500 und Dimension Vista 1500, Siemens PDF, 39KB, File does not meet accessibility standards Date: 13. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03768/13

Corrective action for GlucoMen LX Sensor test strips, Menarini PDF, 443KB, File does not meet accessibility standards Date: 13. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03844/13

Safety Notice for the FrameLink Software, Medtronic PDF, 114KB, File does not meet accessibility standards Date: 13. August 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 03967/13

Safety Notice for the Monaco RTP System, Elekta PDF, 234KB, File does not meet accessibility standards Date: 13. August 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 03037/13

Corrective action for LifeCycle for Prenatal Screening, PerkinElmer PDF, 512KB, File does not meet accessibility standards Date: 13. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04558/13

Corrective action from Epigenomics due to an impaired sample stability PDF, 43KB, File does not meet accessibility standards Date: 13. August 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 04339/13

Batch Recall concerning Burr Hole Latex Free Probe Cover with Gel, Microtek Medical B.V. and Microtek Medical Malta Ltd. PDF, 3MB, File is accessible Date: 12. August 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 04069/13, 04071/13