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Safety Notice for the RPM Respiratory Gating System, Varian Medical Systems PDF, 1MB, File does not meet accessibility standards Date: 21. June 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - nuclear medical therapeutic equipment
Reference 02559/13

Recall for the Oasys Midline Plates, STRYKER PDF, 869KB, File does not meet accessibility standards Date: 21. June 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 02882/13

Safety Notice concerning 5 mm cannula and 5 mm flared cannula, Intuitive Surgical PDF, 111KB, File does not meet accessibility standards Date: 20. June 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03103/13

Lot Recall of the Launcher® Coronary Guide Catheters, Medtronic Inc. PDF, 35KB, File does not meet accessibility standards Date: 20. June 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03268/13

Recall for Dimension® HB1C Flex® Reagent Cartridges, Siemens PDF, 38KB, File does not meet accessibility standards Date: 20. June 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02061/13

Lot Recall of the suture Safil Quick, B. Braun Surgical PDF, 374KB, File does not meet accessibility standards Date: 20. June 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 03033/13

Recall of the Echelon™ 60 Endopath® Stapler Endoscopic Linear Cutter Reload, Ethicon Endo-Surgery PDF, 44KB, File does not meet accessibility standards Date: 20. June 2013 Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 02957/13

Corrective action for Berichrom® PAI, Siemens PDF, 23KB, File does not meet accessibility standards Date: 19. June 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 02644/13

Lot Recall of LINO and DILENE surgical sutures, B. Braun Surgical PDF, 800KB, File does not meet accessibility standards Date: 19. June 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 01878/13

Recall of Parallel Walled Implants, BIOMET 3i PDF, 20KB, File does not meet accessibility standards Date: 19. June 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 02796/13

Safety Notice for the hospital bed Evolution™ LI156, Hill Rom PDF, 23KB, File does not meet accessibility standards Date: 19. June 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 07421/12

Corrective action for the Panbio Dengue IgM Capture Elisa, Alere PDF, 92KB, File does not meet accessibility standards Date: 19. June 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 02540/13

Urgent Safety Notice regarding implantable HeartWare® VAS, HeartWare Inc. PDF, 136KB, File does not meet accessibility standards Date: 19. June 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 03243/13

Safety Notice for the products Brilliance 64, Ingenuity Core and Ingenuity Core128, Philips Healthcare PDF, 198KB, File does not meet accessibility standards Date: 18. June 2013 Type: Customer information

Product group Radiological technology - CT scanners
Reference 02677/13

Urgent Safety Notice for Consulta® CRT-P and Syncra® CRT-P devices, Medtronic PDF, 29KB, File does not meet accessibility standards Date: 18. June 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - cardiac pacemakers
Reference 03240/13

Expanded Safety Notice for the product Berman Angiography catheter, Arrow International PDF, 145KB, File does not meet accessibility standards Date: 18. June 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00056/13

Corrective action for HbA1c Flex® reagent cartridge, Siemens PDF, 25KB, File does not meet accessibility standards Date: 18. June 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02234/13

Corrective action for Advia LSP Calibrator, Siemens PDF, 24KB, File does not meet accessibility standards Date: 18. June 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02029/13

Recall of Lead Cups used for capping of implantable Deep Brain Stimulation Leads (DBS), Medtronic PDF, 150KB, File does not meet accessibility standards Date: 18. June 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 00665/13

Recall for the Epix® and Direct Drive Laparoscopic Graspers, Applied Medical Resources PDF, 2MB, File does not meet accessibility standards Date: 17. June 2013 Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 02827/13

Recall for Synchron System Lactate reagent, Beckman Coulter PDF, 25KB, File does not meet accessibility standards Date: 17. June 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02555/13

Safety Notice concerning Optima C-10 Probetester, Külzer Medizintechnik PDF, 239KB, File does not meet accessibility standards Date: 17. June 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 05292/12

Safety Notice for the software product Praezis Plus version 3.1.x.x, Inomed Medizintechnik PDF, 531KB, File does not meet accessibility standards Date: 17. June 2013 Type: Customer information

Product group Radiological technology - CT scanners
Reference 02547/13

Safety Notice for the Digital Linear Accelerators of type MEVATRON, PRIMUS, ONCOR and ARTISTE, Siemens Healthcare PDF, 158KB, File does not meet accessibility standards Date: 17. June 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 03034/13

Recall for Remel Streptex Group D Latex Reagent, Oxoid PDF, 23KB, File does not meet accessibility standards Date: 17. June 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 02174/13

Lot Recall for the Central Venous Catheter (CVC) Kits, Arrow International Inc. PDF, 74KB, File does not meet accessibility standards Date: 17. June 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 02966/13

Corrective Action / Recall for the R3XLPE Acetabular Liner, Smith & Nephew PDF, 104KB, File does not meet accessibility standards Date: 17. June 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 03050/13

Corrective action for Vidas D-Dimer Exclusion II, Biomerieux PDF, 58KB, File does not meet accessibility standards Date: 14. June 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 02465/13

Safety Notice for the syngo RT Therapist 4.3, Siemens Healthcare PDF, 31KB, File does not meet accessibility standards Date: 14. June 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 03077/13

Expanded Safety Notice for the Maquet Oxygenators - Blood outlet connectors, Maquet Cardiopulmonary AG PDF, 514KB, File does not meet accessibility standards Date: 14. June 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03775/12