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Safety Notice for Trident Acetabular System, Stryker PDF, 141KB, File does not meet accessibility standards Date: 21. September 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03122/09

Recall for Alpha-Fit Stem, Corin PDF, 72KB, File does not meet accessibility standards Date: 21. September 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00562/09

Information for Image Diagnost MammoWorkstations, GE Healthcare PDF, 52KB, File does not meet accessibility standards Date: 18. September 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03318/09

Safety Notice for the Xeno wheelchair, Otto Bock PDF, 59KB, File does not meet accessibility standards Date: 18. September 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02927/09

Urgent Recall for Portex Uncuffed Paediatric Sized Tracheal Tubes, Smith Medical PDF, 454KB, File does not meet accessibility standards Date: 18. September 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03281/09

Safety Notice for several stretchers, Stryker PDF, 128KB, File does not meet accessibility standards Date: 18. September 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 03162/09

Corrective action for ADVIA Centaur® and ADVIA Centaur® XP, Siemens PDF, 24KB, File does not meet accessibility standards Date: 17. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03157/09

Recall for several products because of a packaging error, Angiotech PDF, 556KB, File does not meet accessibility standards Date: 17. September 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03365/09

Recall for PKS SEAL Open Forceps, Gyrus ACMI PDF, 153KB, File does not meet accessibility standards Date: 17. September 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03063/09

Safety Notice for ultrasound system SSD-ALPHA10, ALOKA PDF, 36KB, File does not meet accessibility standards Date: 17. September 2009 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 03120/09

Safety Notice for Enterra Therapy System, Medtronic PDF, 31KB, File does not meet accessibility standards Date: 16. September 2009 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03121/09

Corrective action for Apheresis System MCS+ 9000, Haemonetics PDF, 124KB, File does not meet accessibility standards Date: 16. September 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03269/09

Safety Notice for Varian Proton Therapy Delivery System, Varian PDF, 110KB, File does not meet accessibility standards Date: 16. September 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03069/09

Recall for PlasmaKinetic SuperSect™/PK SuperSect Instrument, Olympus PDF, 80KB, File does not meet accessibility standards Date: 16. September 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02926/09

Safety Notice for Innova 2000 and 4100, GE Healthcare PDF, 61KB, File does not meet accessibility standards Date: 15. September 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03170/09

Further Information about iViewGT 3.4 Service Pack 2 (SP2), Elekta PDF, 57KB, File does not meet accessibility standards Date: 15. September 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03032/09

Information for STERRAD CYCLESURE® and CYCLESURE® 24 Biological Indicator(s), Johnson & Johnson Medical PDF, 147KB, File does not meet accessibility standards Date: 15. September 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03071/09

Recall of defibrillation electrodes, Leonhard Lang PDF, 60KB, File does not meet accessibility standards Date: 15. September 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02224/09

Recall for Contour SE Microspheres, Boston Scientific PDF, 321KB, File does not meet accessibility standards Date: 15. September 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03242/09

Safety Notice for LikoScale 200, 350 and 400, Liko PDF, 126KB, File does not meet accessibility standards Date: 15. September 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 03145/09

Safety Notice for Sutureless Connector (SC) Intrathecal Catheters, Medtronic PDF, 94KB, File does not meet accessibility standards Date: 14. September 2009 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03169/09

Recall for Surgical Cutters according to Lindemann, Hager & Meisinger PDF, 54KB, File does not meet accessibility standards Date: 14. September 2009 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 02800/09

Recall for Renegade Fiber Braided Microcatheter, Renegade Hi-Flo Microcatheter and Renegade Hi-Flo Microcatheter Kits, Boston Scientific PDF, 2MB, File does not meet accessibility standards Date: 14. September 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03222/09

Safety Notice for Hi-Art System, TomoTherapy PDF, 79KB, File does not meet accessibility standards Date: 11. September 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02967/09

Corrective action for Immulite 2000 / 2500 Androstenedione, Siemens PDF, 31KB, File does not meet accessibility standards Date: 11. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03224/09

Safety Notice for Philips IntelliVue Clinical Information Portfolio Release D.0, D.02 and Philips Care Vue Chart Release C.0 PDF, 289KB, File does not meet accessibility standards Date: 11. September 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01306/09

Recall for Ambix activ ambulatory Set and Ambix activ stationary Set, Fresenius Kabi PDF, 17KB, File does not meet accessibility standards Date: 11. September 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02882/09

Safety Notice for Custom Paks, Alcon PDF, 42KB, File does not meet accessibility standards Date: 10. September 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03391/08

Safety Notice for Dimension Vista® System Software Version 3.2.1 or earlier and Dimension Vista® Flex® reagent cartridges, Siemens PDF, 98KB, File does not meet accessibility standards Date: 10. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02643/09

Recall for Restoration Modular cone Bodies, Stryker PDF, 138KB, File does not meet accessibility standards Date: 10. September 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01363/09