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14,984 results

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Recall of specific lots of the ExoSeal™Vascular Closure Device listed below, Cordis Corp. PDF, 203KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 06827/12

Corrective action for Coulter LH 750 and Coulter LH 780 Hematology Analyzer, Beckman Coulter PDF, 314KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 05937/13

Corrective action for the UniCel DxH 800 and 600 Coulter Cellular Analysis System, Beckman Coulter PDF, 538KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 07176/13

Safety Notice for Brivo OEC 715/785/865 C-Arm systems, GE Healthcare PDF, 52KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - mobile radiological diagnostic facilities
Reference 06209/13

Corrective action for Dxl 600 and Access 2, Beckman Coulter PDF, 89KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07168/13

Corrective Action for DELFIA/Auto / DELFIA Enhancement Solution, PerkinElmer PDF, 3MB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06331/13

Urgent Safety Information for the product Incor® Control Unit, Berlin Heart GmbH PDF, 796KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 07041/13

Corrective Action for LIAISON Control Mumps IgG, DiaSorin PDF, 1MB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 06266/13

Safety Notice for Artis systems running software version VC21B, Siemens Healthcare PDF, 2MB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 06725/13

Safety Notice for OsseoCare Pro iPad® app software release 1.2.0.7, Bien‐Air Dental PDF, 144KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Dental products - equipment
Reference 06396/13

Safety Notice for Brilliance CT Big Bore Oncology, Brilliance CT Big Bore Radiology and Brilliance CT 16 (Air) systems, Philips PDF, 178KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 05770/13

Corrective action for Vitros Immunodiagnostic Products CA 125 II Calibrators, Ortho PDF, 166KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 06142/13

Corrective action for Vitros Chemistry Products Na+ Slides und Vitros Chemistry Products Calibrator Kit 2, Ortho PDF, 264KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06355/13

Safety Notice for qLabs PT-INR Q-1 Pro Test Systems, nal von minden PDF, 619KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00466/13

Safety Notice for Vivid E9 4D ultrasound system, GE Healthcare PDF, 71KB, File does not meet accessibility standards Date: 17. December 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 06624/13

Safety Notice for dental chair A-dec 200, A-dec PDF, 462KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 04663/13

Safety Notice for Elekta motorized wedges in RayStation 3.0, 3.5 and 4.0, RaySearch Laboratories PDF, 110KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 06352/13

Safety Notice concerning the Manual Film Composer Issue on Brivo CT315/325, Brivo CT385, Optima CT520 and Optima CT540, GE Healthcare PDF, 55KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 06534/13

Safety Notice for Discovery NM/CT670, Optima NM/CT640, Discovery NM630 and Brivo NM615, GE Healthcare PDF, 47KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 06399/13

Updated Safety Notice concerning the automated Blood Collection, Terumo PDF, 66KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 02797/13

Safety notice for insulin pumps DANA Diabecare IIS, Sooil Development Co. Ltd PDF, 727KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 02825/13

Safety Notice concerning the Hamilton-C2 ventilator, Hamilton Medical PDF, 2MB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05825/13

Safety Notice for Surgical Kits about the change of sterilization instructions, BIOMET 3i PDF, 119KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 06464/13

Safety Notice concerning the Puritan Bennett™ 840 ventilator, Covidien PDF, 152KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 07326/13

Safety Notice concerning Eclipse™ Treatment Planning System, ARIA® Radiation Oncology, ARIA®Radiation Therapy Management, and Acuity™, Varian medical systems PDF, 32KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 07371/13

Safety Notice for the Basin Liner within Mölnlycke ProcedurePak®, Mölnlycke Health Care PDF, 342KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - others
Reference 05954/13

Safety Notice concerning DRX-Evolution and KODAK DirectView X-ray systems, Carestream Health PDF, 18KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 07207/13

Recall for the Drill Templates and Saw Guides for LCP-Ulna-Osteotomyplates 2.7, Synthes GmbH PDF, 65KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06986/13

Recall Removal of the Vessix™ Generator System, Boston Scientific Corp. PDF, 158KB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 06855/13

Safety Notice for Dialox 10 kg, Bioxal SA PDF, 2MB, File does not meet accessibility standards Date: 16. December 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 06290/13