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Safety Notice for the Patient Data Module (PDM) – Mounting Latch Failure, GE Healthcare PDF, 50KB, File does not meet accessibility standards Date: 22. April 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 02280/14

Safety Notice for the product syngo Dynamics with Sensis integration licence, Siemens Healthcare, Siemens Healthcare PDF, 2MB, File does not meet accessibility standards Date: 22. April 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 01417/14

Safety Advisory Notice for the Axiom Luminos dRF system for fluoroscopy and radiography, Siemens Healthcare PDF, 55KB, File does not meet accessibility standards Date: 22. April 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 02035/14

Safety Notice concerning OR-Table-System OTESUS 1160.01, Maquet GmbH PDF, 958KB, File does not meet accessibility standards Date: 22. April 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02223/14

Safety Notice for the ExacTrac 5.5.5 Patient Positioning System, Brainlab AG PDF, 717KB, File does not meet accessibility standards Date: 22. April 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 02127/14

Safety Notice for the LenSx® Laser System, Alcon Pharma GmbH PDF, 141KB, File does not meet accessibility standards Date: 22. April 2014 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 02073/14

Recall of several lots of the Cadisc®-L Artificial Spinal Discs, RANIER PDF, 66KB, File does not meet accessibility standards Date: 17. April 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 01923/14

Safety Notice for the product IMTEC-CIC IgG ELISA, HUMAN Gesellschaft für Biochemica und Diagnostica mbH PDF, 229KB, File does not meet accessibility standards Date: 17. April 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 01636/14

Recall of certain lots of two products (Pipeline Embolization Device and Alligator Retrieval Device), COVIDIEN PDF, 94KB, File does not meet accessibility standards Date: 17. April 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 02092/14

Recall for Trigen Intertan Nails, Smith & Nephew PDF, 89KB, File does not meet accessibility standards Date: 16. April 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 02033/14

Corrective action of the surgical lights PowerLED 700 and H LED 700, Maquet PDF, 1MB, File does not meet accessibility standards Date: 16. April 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 01168/14

Urgent Safety Notice for Axiom Artis or Artis zee systems in connection with hand switch, Siemens Healthcare PDF, 22KB, File does not meet accessibility standards Date: 16. April 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 00497/14

Urgent Safety Notice for the 550 TxT Treatment Table of the Digital Linear Accelerator (LINAC), Siemens Healthcare PDF, 18KB, File does not meet accessibility standards Date: 16. April 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 01718/14

Important Safety Notice for AXIOM Artis, Artis zee or Artis Q systems, Siemens Healthcare PDF, 1MB, File does not meet accessibility standards Date: 16. April 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 02022/14

Safety Notice concerning the sterEOS workstation, EOS PDF, 276KB, File does not meet accessibility standards Date: 16. April 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 02021/14

Otto Bock: Safety Information for the A200 Power Wheelchair, Skippi / Skippi Plus Power Wheel chair PDF, 212KB, File does not meet accessibility standards Date: 15. April 2014 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - mobility aids
Reference 01975/14

Recall of one lot of the Optivac Knee Nozzle, Biomet France SARL PDF, 47KB, File does not meet accessibility standards Date: 15. April 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 01454/14

Urgent Safety Notice for the GLOBAL® APG+ 2,5 mm Breakaway Guide Pin, DePuy Synthes PDF, 3MB, File does not meet accessibility standards Date: 15. April 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02017/14

Safety Notice for the EFK Knee-System, OHST Medizintechnik AG PDF, 3MB, File does not meet accessibility standards Date: 15. April 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 02019/14

Recall of three lots of the Astron Pulsar Self-Expanding Nitinol Stent System, Biotronik AG PDF, 38KB, File does not meet accessibility standards Date: 15. April 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 01968/14

Safety Notice concerning Vital Signs Breathing Circuits, GE Healthcare PDF, 86KB, File does not meet accessibility standards Date: 15. April 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 01668/14

Safety Notice for the Perceval S Post-Dilation Catheter Size M, Sorin Group PDF, 3MB, File does not meet accessibility standards Date: 15. April 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 07999/13

Urgent Safety Notice for the ADAC Vertex Classic, Vertex Plus, Solus and Vertex V60 Systems, Philips Healthcare PDF, 675KB, File does not meet accessibility standards Date: 15. April 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 02040/14

Recall of several Weck® Vista™ laparoscopic Ports, Teleflex PDF, 172KB, File does not meet accessibility standards Date: 14. April 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - visceral surgery
Reference 01458/14

DePuy Synthes: Urgent Safety Information concerning the Guide Wire Ø 3,2mm, length 400mm PDF, 257KB, File does not meet accessibility standards Date: 14. April 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 01960/14

Updated Reprocessing Procedure for unsterile surgical needles and cannulas, Ernst Kratz GmbH PDF, 735KB, File does not meet accessibility standards Date: 14. April 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 05420/13

Recall of one batch number of the product i-Visc 1.4, i-Medical Ophthalmic International GmbH PDF, 543KB, File does not meet accessibility standards Date: 14. April 2014 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - liquid media for ophthalmological purposes
Reference 01678/14

Lot Recall for the Surfix Screw, NEWDEAL SAS PDF, 601KB, File does not meet accessibility standards Date: 14. April 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 01949/14

Recall of several batches of the products Propano AF® and esteer® SEPT, Esteer Pharma GmbH PDF, 625KB, File does not meet accessibility standards Date: 14. April 2014 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 00228/14

Safety Notice for the ACUSON X700 ultrasound systems, Siemens PDF, 6MB, File does not meet accessibility standards Date: 14. April 2014 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 02003/14