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Safety Notice for the Allura Xper FD20 Biplane und Allura Xper FD 20 Biplane OR Table, Philips Healthcare PDF, 829KB, File does not meet accessibility standards Date: 01. March 2013 Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 00664/13

Corrective Action for Dimension IBCT Flex Reagent Cartridge DF 84, Siemens PDF, 104KB, File does not meet accessibility standards Date: 01. March 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00005/13

Corrective Action for Innovacon, SureStep and Instalert Drug of Abuse Tests Product Insert – French Language Version, Innovacon Inc. PDF, 105KB, File does not meet accessibility standards Date: 01. March 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07570/12

Urgent Safety Notice for the Eclipse™ Treatment Planning System, Varian Medical Systems PDF, 2MB, File does not meet accessibility standards Date: 01. March 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 00530/13

Recall Information: Curapor transparent, Curafix i.v. control and Raucodrape Inzisionsfolie, Lohmann & Rauscher PDF, 745KB, File does not meet accessibility standards Date: 01. March 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - bandages
Reference 00910/13

Urgent Safety Notice for the V-CAS™ Catheter Advancement System and V-CAS Deflect™, Stereotaxis PDF, 301KB, File does not meet accessibility standards Date: 28. February 2013 Type: Customer information

Product group Radiological technology - navigation systems
Reference 00620/13

Recall for Mueller Hinton Agar with Horse Blood, Oxoid PDF, 84KB, File does not meet accessibility standards Date: 28. February 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 00437/13

Recall for the WSI MX/PX-Titan® Expertise and WSI MX/PX-Titan® Expertise Integration, PETER BREHM PDF, 177KB, File does not meet accessibility standards Date: 28. February 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 07384/12

Safety Notice for the SureSigns patient monitors, Philips Healthcare PDF, 308KB, File does not meet accessibility standards Date: 28. February 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 00564/13

Recall for Firebird Spinal Fixation System Parallel Rod Connectors and Axial Rod Connectors, ORTHOFIX PDF, 149KB, File does not meet accessibility standards Date: 28. February 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 00578/13

Recall for GHI 154, MediRox PDF, 69KB, File does not meet accessibility standards Date: 28. February 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00265/13

Lot Recall for Bio ACL Screws, BioZip Anchors, XCEL Anchors, STRYKER PDF, 166KB, File does not meet accessibility standards Date: 28. February 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 00676/13

Recall for Instrument Manager v8.12.01, Data Innovations PDF, 50KB, File does not meet accessibility standards Date: 27. February 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06211/12

Corrective Action for VITROS Chemistry Products Vapor Adsorption Cartridge, Ortho Clinical Diagnostics PDF, 357KB, File does not meet accessibility standards Date: 27. February 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07834/12

Recall for CardioProfiler and Profiler SOB, Alere PDF, 116KB, File does not meet accessibility standards Date: 27. February 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 05811/12

Urgent Safety Notice for the PHAROS VITESSE Neurovascular Stent System, BIOTRONIK AG PDF, 3MB, File does not meet accessibility standards Date: 27. February 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 00601/13

Recall for ARCHITECT 25-OH Vitamin D, Abbott PDF, 30KB, File does not meet accessibility standards Date: 27. February 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07715/12

Recall for the cannulated screwdriver and screwdriver tip, Newdeal SAS PDF, 1MB, File does not meet accessibility standards Date: 27. February 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00619/13

Safety Notice concerning a corrective action of the HeartStart XL+ monitor/defibrillators, Philips Healthcare PDF, 110KB, File does not meet accessibility standards Date: 27. February 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 00556/13

Recall for Cerascreen, DST Diagnostische Systeme und Technologien PDF, 122KB, File does not meet accessibility standards Date: 26. February 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 02741/12

Recall for ABX Diluent 20L, Horiba PDF, 103KB, File does not meet accessibility standards Date: 25. February 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00467/13

Lot Recall of the CT ASPHINA 409MP intraocular lens, Carl Zeiss Meditec PDF, 122KB, File is accessible Date: 25. February 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 00572/13

Safety Notice for the Spacers for Delta liners in Delta acetabular System, LimaCorporate PDF, 181KB, File does not meet accessibility standards Date: 25. February 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 00659/13

Lot Recall of the Cathether Mount with Superset tube (Micro Mount 15M-15F), Intersurgical Ltd. PDF, 119KB, File does not meet accessibility standards Date: 25. February 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 00627/13

Recall for Medonic CA Lyse 10 L, Boule Medical AB PDF, 2MB, File does not meet accessibility standards Date: 22. February 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 06551/12

Safety Notice for syngo Workflow MLR, Siemens Healthcare PDF, 3MB, File does not meet accessibility standards Date: 22. February 2013 Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 00330/13

Recall for IRON Calibrator, Siemens PDF, 30KB, File does not meet accessibility standards Date: 22. February 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00054/13

Recall for VIDAS D-Dimer Exclusion II Kit, BioMerieux PDF, 49KB, File does not meet accessibility standards Date: 22. February 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00052/13