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Recall of the Fusion OMNI ERCP Catheter from Cook Endoscopy PDF, 33KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03379/06

Recall of Preface Sheaths from Biosense Webster PDF, 66KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03495/06

Information concerning the Codman Hakim valve programmers from Ethicon PDF, 93KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01777/06

Customer Information for several products of Thomashilfen GmbH PDF, 56KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 03027/06

Safety Information concerning the Proteus XR/a, Revolution XR/d and Definium 8000 X-ray systems from GE Healthcare PDF, 268KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01094/06

Recall of Frazier and Poole Suction Instruments from ConMed PDF, 88KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03446/06

Corrective actions concerning the Dimension Articulated Stone Baskets from Bard PDF, 65KB, File does not meet accessibility standards Date: 20. December 2006 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03570/06

Information from Siemens concerning examinations which are opened under RIS control PDF, 63KB, File does not meet accessibility standards Date: 20. December 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03250/06

Information concerning the BrainSCAN version 5.2 or higher from BrainLAB PDF, 61KB, File does not meet accessibility standards Date: 20. December 2006 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03316/06

Recall of the BCI Autocorr Patientmonitors from Smiths Medical PDF, 105KB, File does not meet accessibility standards Date: 20. December 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03480/06

Recall of the Lumenis DuoTome SideLite™ 550 Micron Delivery System from Lumenis PDF, 107KB, File does not meet accessibility standards Date: 20. December 2006 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03102/06

Corrective action for the Cell-Dyn 22 Calibrator and Cell-Dyn 22 Control from Abbott PDF, 138KB, File does not meet accessibility standards Date: 19. December 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03313/06

Information concerning the Picture Archiving and Communication System (PACS) syngo Imaging from Siemens PDF, 72KB, File does not meet accessibility standards Date: 19. December 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02701/06

Recall of the VAC Instill vacuum tubing from KCI Medical Products PDF, 53KB, File does not meet accessibility standards Date: 19. December 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03122/06

Information concerning the iPlan RT Image versions 2.0 or 3.0 from BrainLAB PDF, 62KB, File does not meet accessibility standards Date: 19. December 2006 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03496/06

Corrective action for the Amax Destiny Plus coagulation analyzers from Trinity Biotech PDF, 602KB, File does not meet accessibility standards Date: 19. December 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02830/06

Corrective action and recall for the MicroScan LabPro Information Manager System from Dade Behring PDF, 42KB, File does not meet accessibility standards Date: 19. December 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03429/06

Recall of certain connectors from Fisher & Paykel PDF, 41KB, File does not meet accessibility standards Date: 19. December 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03454/06

Recall of QUATTROcare spray cans from KaVo Dental PDF, 266KB, File does not meet accessibility standards Date: 19. December 2006 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 03603/06

Recall of TraXis Fixed Trial Rod and Rasp instruments from Abbott Spine PDF, 39KB, File does not meet accessibility standards Date: 19. December 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03605/06

Inspection of the trolley chassis of the Fabius GS anaesthesia devices from Dräger PDF, 40KB, File does not meet accessibility standards Date: 12. December 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02869/06

Corrective action or the N Latex HCY (OPAX03) Assay on the BN™ II System from Dade Behring PDF, 47KB, File does not meet accessibility standards Date: 12. December 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03373/06

Corrective action for the Lipase reagent OSR6x30 from Olympus PDF, 55KB, File does not meet accessibility standards Date: 12. December 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03295/06

Information for the Centiva/5 and the Centiva/5 Plus critical care ventilators from GE Healthcare PDF, 182KB, File does not meet accessibility standards Date: 12. December 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03251/06

Recall of Cord Cells with the lot number 374.188 from Medion PDF, 49KB, File does not meet accessibility standards Date: 08. December 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03161/06

Refitting of the patient hoists model Minerva from Arjo PDF, 28KB, File does not meet accessibility standards Date: 08. December 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02072/04

Recall of the ConMed Electrosurgery System 5000 Electrosurgical Generator PDF, 65KB, File does not meet accessibility standards Date: 08. December 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02805/06

Corrective action for BacT/Alert systems from bioMérieux PDF, 175KB, File does not meet accessibility standards Date: 08. December 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03357/06