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14,979 results

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Urgent Safety Notice for Digital Linear Accelerators of type MEVATRON™ and PRIMUS™ with Automatic Sequenced Treatment Delivery Option, Siemens AG PDF, 22KB, File does not meet accessibility standards Date: 15. December 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 03315/14

Urgent Safety Notice for the Embru LINEA Hospital Beds, Embru-Werke AG PDF, 265KB, File does not meet accessibility standards Date: 12. December 2014 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 06859/14

Corrective action for the Philips HeartStart MRx Monitor/Defibrillator, Philips Healthcare PDF, 166KB, File does not meet accessibility standards Date: 12. December 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 08094/14

Corrective action for the Philips HeartStart MRx Monitor/Defibrillator, Philips Healthcare PDF, 224KB, File does not meet accessibility standards Date: 12. December 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 08099/14

Corrective action for the Philips Model EPIQ 5 Ultrasound System, Philips Healthcare PDF, 178KB, File does not meet accessibility standards Date: 12. December 2014 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 08090/14

Corrective action for the BrightView XCT system, Philips Healthcare PDF, 197KB, File does not meet accessibility standards Date: 12. December 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 07999/14

Urgent Safety Notice for the Puritan Bennett™ 980 Series Ventilator System, Covidien PDF, 46KB, File does not meet accessibility standards Date: 12. December 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07249/14

Urgent Safey Notice for the MetaVision® Suite, Clinical Information System version 5.4x, iMDsoft Ltd. PDF, 392KB, File does not meet accessibility standards Date: 12. December 2014 Topics: Medical devices Type: Customer information

Product group Medical data processing (software) - others
Reference 07822/14

Recall for the THERMOCOOL SMARTTOUCH® SF Katheter, Biosense Webster / Johnson & Johnson MEDICAL NV/SA PDF, 8MB, File does not meet accessibility standards Date: 12. December 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07939/14

Urgent Safety Notice for the Drill set long, drill stop compatible for D 4.8mm Implant, Institut Straumann PDF, 15KB, File does not meet accessibility standards Date: 12. December 2014 Topics: Medical devices Type: Customer information

Product group Dental products - instruments
Reference 07207/14

Safety Notice for the VERO™/MHI-TM2000 Linear Accelerator System, Mitsubishi Heavy Industries, Ltd. PDF, 3MB, File does not meet accessibility standards Date: 12. December 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 07643/14

Corrective action for Philips M1783A and M5526A Sync Cables, Philips Healthcare PDF, 188KB, File does not meet accessibility standards Date: 10. December 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 08091/14

Recall for the PF Stem lateralized cemented size 8 and PF Stem Standard cemented Size 7, Zimmer PDF, 139KB, File does not meet accessibility standards Date: 10. December 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07959/14

Corrective action for a limited number of dental implants, BIOMET 3i PDF, 102KB, File does not meet accessibility standards Date: 10. December 2014 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 07765/14

Recall for the product ArthroCare Ambient HipVac 50 Wand, ArthroCare Corp./Smith & Nephew PDF, 270KB, File does not meet accessibility standards Date: 10. December 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 07625/14

Important Safety Notice for the Vena Cava Filter Sets, Cook Medical PDF, 140KB, File does not meet accessibility standards Date: 10. December 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 07981/14

Urgent Safety Notice for the Accu-Chek Connect Diabetes Management App, Roche Diagnostics PDF, 123KB, File does not meet accessibility standards Date: 10. December 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 07227/14

Corrective action for the products TC-PLUS™ Tibial Resection Guide proximal, VKS Tibia Guide proximal EU, Smith & Nephew PDF, 72KB, File does not meet accessibility standards Date: 09. December 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 08054/14

Urgent Safety Notice for the Breas Vivo 60 Home Care Ventilator, Breas Medical AB PDF, 91KB, File does not meet accessibility standards Date: 09. December 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07950/14

Recall for the product MicroVue Bb Plus EIA, Quidel PDF, 282KB, File does not meet accessibility standards Date: 09. December 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07008/14

Corrective action for the product ImmunoCAP ISAC sIgE 112, Phadia AB / Thermo Fisher Scientific PDF, 75KB, File does not meet accessibility standards Date: 09. December 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 06808/14

Recall for some units of Dafilon Blue, B. Braun Surgical / Lohmann & Rauscher GmbH & Co. KG PDF, 83KB, File does not meet accessibility standards Date: 09. December 2014 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 07821/14

Corrective action for Dimension® Theophylline (THEO) Flex® Reagent Cartridge Lots BA5134 and BA5162, Siemens Healthcare PDF, 25KB, File does not meet accessibility standards Date: 09. December 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07836/14

Corrective action for the Syringe pump green stream SY-P ARGUS 600, Firmware version 1.00 - 1.51 / ARGUS 600, Firmware version 3.01 - 4.32, CODAN ARGUS AG PDF, 1MB, File does not meet accessibility standards Date: 09. December 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 07662/14

Corrective action for the product BRONCHIAL DOUBLE LUMEN TUBE SET, Teleflex Medical PDF, 186KB, File does not meet accessibility standards Date: 09. December 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07943/14

Corrective action for the CARDIOSAVE® Hybrid Intra-Aortic Balloon Pump (IABP), Maquet / Datascope Corp. PDF, 53KB, File does not meet accessibility standards Date: 09. December 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07638/14

Recall for LENTIS HydroSmart foldable Intraocular lenses in glass vials, Oculentis GmbH PDF, 39KB, File does not meet accessibility standards Date: 08. December 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 08056/14

Recall for the ARROW® Continuous Nerve Block Needle, ARROW International Inc. PDF, 218KB, File does not meet accessibility standards Date: 08. December 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - injection kits
Reference 07693/14

Recall for the Guide Wire Semislip, Urotech PDF, 31KB, File does not meet accessibility standards Date: 08. December 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07811/14

Urgent Safety Notice for the DRX-Revolution Mobile X-Ray System, Carestream Health, Inc. PDF, 132KB, File does not meet accessibility standards Date: 08. December 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - mobile radiological diagnostic facilities
Reference 07851/14