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Field Safety Notice concerning the external pacemakers EDP 30/A and EDP 30/S as well as VK-99 cable PDF, 25KB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04581/08

Field Safety Notice concerning the Panda iRes and Giraffe Bedded Warmers PDF, 1MB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 04759/08

Field Safety Notice of Leksell GammaPlan and Leksell SurgiPlan PDF, 105KB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04767/08

Recall of S4 FW258R K-Wire-Guidung Instrument for Set S4 SC from manufacturer Aesculap AG Tuttlingen PDF, 567KB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 04786/08

Field Safety Notice of Siemens of AXIOM Iconos R200 ND X-ray system PDF, 668KB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04789/08

TomoTherapy has issued a Field Safety Notice about a possible error in the irradiation by Hi-type systems PDF, 1MB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03614/08

TomoTherapy has issued a Field Safety Notice about a possible error in the irradiation by Hi-type systems PDF, 4MB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03904/08

Information of Mini Bypass Bag of Sorin Group Italia PDF, 489KB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04825/08

Recall of Quadrox-i Oxygenators PDF, 515KB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04816/08

Recall of Cellabs Pty Ltd. for Pneumo Cel IFA Kit PDF, 1,023KB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04811/08

Field Safety Notice concerning Mammographie X-ray system Diamond PDF, 248KB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04803/08

Field Safety Notice concerning a Corpuls 3 Defibrillator/Monitoring systems PDF, 221KB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03838/08

Field Safety Notice about corrective actions concerning STERRAD 100S Sterilizer PDF, 1MB, File does not meet accessibility standards Date: 13. January 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 04429/08

Recall of Biomérieux for Selenit F Bouillon PDF, 1MB, File does not meet accessibility standards Date: 12. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04494/08

Recall of Pentapharm extended for reagents ex-TEM PDF, 2MB, File does not meet accessibility standards Date: 12. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04476/08

Follow-up of the Corrective Action of Abbott for ACCELERATOR APS Centrifuge Module PDF, 1MB, File does not meet accessibility standards Date: 12. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03537/08

Field Safety Notice concerning CT Scanner PRESTO and ECLOS from Hitachi Medical PDF, 234KB, File does not meet accessibility standards Date: 12. January 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04824/08

Field Safety Notice concerning a potential leak in the Pulmonary Toolkit and Big Bore from Philips Healthcare PDF, 29KB, File does not meet accessibility standards Date: 12. January 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04801/08

Recall of Biomérieux for VITEK 2 GN PDF, 1MB, File does not meet accessibility standards Date: 12. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04627/08

Corrective Action of Beckman Coulter for Power Processor with LX Connections PDF, 1MB, File does not meet accessibility standards Date: 12. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04376/08

Recall of Siemens Healthcare Diagnostics for Quadriga BeFree System PDF, 458KB, File does not meet accessibility standards Date: 12. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04556/08

Recall of Olympus for Ferritin reagent PDF, 458KB, File does not meet accessibility standards Date: 12. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04550/08

Recall of OXOID Deutschland / Thermo Fisher Scientific for Horse Serum PDF, 1,014KB, File does not meet accessibility standards Date: 12. January 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04362/08

Recall of lot numbers of a OP set from Mölnlycke Health Care PDF, 1MB, File does not meet accessibility standards Date: 12. January 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04777/08

Recall for EL-Cups, OHST Medizintechnik AG PDF, 49KB, File does not meet accessibility standards Date: 08. January 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03354/08

Information for Gamma3 Trochanteric Nail, Stryker PDF, 332KB, File does not meet accessibility standards Date: 08. January 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04810/08

Safety Notice for Fred easy and Fred Easy Paediatric, Schiller PDF, 274KB, File does not meet accessibility standards Date: 07. January 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04479/08

Safety Notice for SynchroMed EL and SynchroMed II, Medtronic PDF, 373KB, File does not meet accessibility standards Date: 07. January 2009 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03292/08

Recall for CardioVations EndoClamp Aortic Catheter, Edwards Lifesciences PDF, 115KB, File does not meet accessibility standards Date: 07. January 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04765/08

Recall for NexGen Complete Knee Solution-Provisional Articular Surface, Zimmer Inc. PDF, 81KB, File does not meet accessibility standards Date: 07. January 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 04772/08