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Corrective Action for ABL 90 FLEX, Radiometer PDF, 21KB, File does not meet accessibility standards Date: 03. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04451/12

Safety Notice concerning MR290 Autofeed Humidification Chambers, Fisher & Paykel PDF, 55KB, File does not meet accessibility standards Date: 03. August 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05042/12

Safety Corrective Action regarding Eon Mini model 65-3788 and Brio model 65-6788, St. Jude Medical PDF, 74KB, File does not meet accessibility standards Date: 03. August 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 04939/12

Safety Notice for the Brilliance series 6, 16, 40, 64, CT Big Bore, iCT and iCT SP CT systems, Philips Healthcare PDF, 85KB, File does not meet accessibility standards Date: 02. August 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 04978/12

Corrective Action for Techno TwinStation, Bio-Rad PDF, 657KB, File does not meet accessibility standards Date: 02. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 04019/12

Safety Notice for the EVG Videogastroskop ENDOMED-DUO and EVC 21-37 Videocoloskop ENDOMED-DUO, ESCAD PDF, 75KB, File does not meet accessibility standards Date: 02. August 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 01352/12

Recall for the sterile Teflon Tube T2 Humerus, Stryker Osteosynthesis PDF, 60KB, File does not meet accessibility standards Date: 02. August 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04983/12

Safety Corrective Action regarding EXCOR arterial cannula with graft CGRG-021, Berlin Heart GmbH PDF, 1MB, File does not meet accessibility standards Date: 02. August 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 05000/12

Corrective action for BacT/Alert, BioMerieux PDF, 319KB, File does not meet accessibility standards Date: 01. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 01925/12

Recall of VariSource™ IX and 200 series Nucletron Adapter and Transfer Guide Tube and Set, Varian medical systems PDF, 1MB, File does not meet accessibility standards Date: 01. August 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - nuclear medical therapeutic equipment
Reference 02518/12

Lot Recall for the Shiley Reusable Cannual cuffed Tracheostomy Tubes, Covidien PDF, 904KB, File does not meet accessibility standards Date: 01. August 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 04837/12

Safety Notice for the Leica M525 F50 surgical microscope, Leica PDF, 241KB, File does not meet accessibility standards Date: 01. August 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 03865/12

Medical Device Recall: NC / RC Screws for CARES Abutment, STRAUMANN PDF, 44KB, File does not meet accessibility standards Date: 31. July 2012 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 04591/12

Safety Notice regarding syngo Dynamics regional settings for “decimal separator”, Siemens Healthcare PDF, 305KB, File does not meet accessibility standards Date: 31. July 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04713/12

Recall concerning DYNAMOMETRIC T handle, Kisco International PDF, 46KB, File does not meet accessibility standards Date: 30. July 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04862/12

Safety Notice for BVI CustomEyes Ophthalmic Procedure Kits, Beaver-Visitec International PDF, 72KB, File does not meet accessibility standards Date: 30. July 2012 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 04818/12

Information about the Instructions for Use for the EG-3870UTK Ultrasound Video Gastroscope, Pentax PDF, 94KB, File does not meet accessibility standards Date: 30. July 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 04520/12

Safety Notice concerning a corrective action of the defibrillators cardiolife TEC-8300K series, Nihon Kohden Europe GmbH PDF, 93KB, File does not meet accessibility standards Date: 30. July 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 04783/12

Medical Device Alert for all model and lot numbers of the Clampholder for neonates and paediatric endotrachealtubes of the manufacturer EMS Medical Group Ltd., UK PDF, 60KB, File does not meet accessibility standards Date: 30. July 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 04838/12

Lot Recall for Biomet Bone Cement V, BIOMET PDF, 177KB, File does not meet accessibility standards Date: 27. July 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - materials for implants
Reference 04533/12

Recall for MicroCool breathable surgery gowns, Kimberly Clark PDF, 143KB, File does not meet accessibility standards Date: 27. July 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04733/12

Safety Notice for Mustang walking aids, R 82 A/S PDF, 71KB, File does not meet accessibility standards Date: 27. July 2012 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - daily living aids
Reference 04629/12

Corrective Action for ADVIA Centaur / ADVIA Centaur XP, Siemens PDF, 30KB, File does not meet accessibility standards Date: 27. July 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 04745/12

Safety Notice for the Perimeter OCTOPUS 101, Haag-Streit International PDF, 477KB, File does not meet accessibility standards Date: 27. July 2012 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological diagnostics
Reference 04597/12

Recall of Radiofrequency Cannulae, Stryker PDF, 69KB, File does not meet accessibility standards Date: 26. July 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 04804/12

Corrective Action of DiaSys for one HbA1c IS, for one HbA1c FS, TruCal HbA1c liquid, TruLab HbA1c Level 1 and TruLab HbA1c Level 2, DiaSys PDF, 195KB, File does not meet accessibility standards Date: 26. July 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04650/12

Field Safety Corrective Action for the OctoNova Hemofiltration Device, Nikkiso Europe GmbH PDF, 373KB, File does not meet accessibility standards Date: 26. July 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 01343/12

Safety Notice regarding Integra Cerebro Spinal Fluid management devices / Instructions for Use, Integra Neuro Science PDF, 143KB, File does not meet accessibility standards Date: 25. July 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03296/12

Recall for VIDAS EBV VCA-EA IgG, BioMérieux SA PDF, 61KB, File does not meet accessibility standards Date: 25. July 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 04542/12

Recall for CALIBRATOR 80, ARKRAY PDF, 222KB, File does not meet accessibility standards Date: 25. July 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01018/12