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14,979 results

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Recall of ETHICON VICRYL™ Suture, Johnson & Johnson International PDF, 155KB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 02152/15

Urgent Safety Notice for Medtronic Neuromodulation DBS system extensions, Medtronic Inc. PDF, 256KB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 02328/15

Corrective action for the ISKD - Intramedullary Skeletal Kinetic Distractor (Limb Lengthener), Orthofix Inc. PDF, 157KB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 01085/15

Recall for the Retrograde Cardioplegia Cannula, ANDOCOR n.v. PDF, 2MB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 02080/15

Corrective action for the Lotus™ Valve System, Boston Scientific PDF, 304KB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - cardiac surgery
Reference 02291/15

Corrective action for the Fem-Flex II Femoral Arterial Cannulae, Edwards Lifesciences Services GmbH/Maquet Cardiopulmonary AG PDF, 100KB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 02265/15

Urgent Safety Notice for the Biosense Webster’s SMARTABLATE™ Generator System manufactured by Stockert GmbH PDF, 136KB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 01733/15

Recall of two batches of the Neumann Titan Arthrodesis Plate Proximal, Zimmer GmbH on behalf of Normed Medizin-Technik GmbH PDF, 275KB, File does not meet accessibility standards Date: 20. April 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 02201/15

Safety Notice for the AQT90 FLEX Analyzer, Radiometer PDF, 65KB, File does not meet accessibility standards Date: 20. April 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01738/15

Corrective action for the ADVIA® Chemistry Systems/ADVIA Chemistry Lipase, Siemens Healthcare Diagnostics PDF, 218KB, File does not meet accessibility standards Date: 20. April 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02046/15

Corrective action for the ADVIA Centaur® XPT System, Siemens Healthcare Diagnostics PDF, 105KB, File does not meet accessibility standards Date: 20. April 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02067/15

Safety Notice for the Primus RS Worksimulator, BTE Technologies, Inc. PDF, 167KB, File does not meet accessibility standards Date: 20. April 2015 Topics: Medical devices Type: Customer information

Product group Physical therapy - massage / mobility devices
Reference 01120/15

Safety Notice for the Thermablate EAS System, Idoman Teoranta PDF, 356KB, File does not meet accessibility standards Date: 20. April 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02257/15

Corrective action for the FLOW-i C20 - C40 Anaesthesia system, Maquet Critical Care AB PDF, 103KB, File does not meet accessibility standards Date: 20. April 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 02018/15

Urgent Safety Notice/Corrective action for various GE Healthcare MRI systems, GE Healthcare PDF, 74KB, File does not meet accessibility standards Date: 20. April 2015 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 02032/15

Further Information/Corrective action for the T2100 and T2000 Treadmills, GE Healthcare PDF, 145KB, File does not meet accessibility standards Date: 16. April 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - functional diagnostics by way of gas exchange and exercise
Reference 02108/15

Urgent Safety Notice for the SynchroMed® II Implantable Drug Infusion Pump, Medtronic PDF, 99KB, File does not meet accessibility standards Date: 16. April 2015 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - drug pumps
Reference 02149/15

Corrective action for the T2100 Treadmill (Uncontrolled Walking Belt Motion), GE Healthcare PDF, 155KB, File does not meet accessibility standards Date: 16. April 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - functional diagnostics by way of gas exchange and exercise
Reference 02109/15

Corrective action for Dade® Actin® Activated Cephaloplastin Reagent, Siemens Healthcare Diagnostics PDF, 10MB, File does not meet accessibility standards Date: 15. April 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 01506/15

Corrective action for the Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT, Axis-Shield Diagnostics Limited PDF, 300KB, File does not meet accessibility standards Date: 15. April 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01837/15

Urgent Safety Notice for the Liquid Urine Control Level 2, Randox Laboratories Ltd. PDF, 106KB, File does not meet accessibility standards Date: 15. April 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00836/15

Corrective action for the ExacTrac 6.x Patient Positioning System, Brainlab AG PDF, 162KB, File does not meet accessibility standards Date: 15. April 2015 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 02117/15

Recall for the Irrigation syringe 100/120ml, Asid Bonz GmbH PDF, 219KB, File does not meet accessibility standards Date: 15. April 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 01722/15

Corrective action for the Manual Collimator Exchange system in use with an ADAC Vertex Plus, CARDIO, Solus or Vertex V60 imaging system, Philips Healthcare PDF, 317KB, File does not meet accessibility standards Date: 15. April 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 02119/15

Recall for the Urethra pessary, size 55mm, Dr. Arabin GmbH & Co. KG PDF, 95KB, File does not meet accessibility standards Date: 14. April 2015 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - care of natural and artificial body orifices
Reference 02042/15

Urgent Safety Notice for the Rehaforum Rollator with Eurobrake Silver, Rehaforum Medical PDF, 196KB, File does not meet accessibility standards Date: 14. April 2015 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - daily living aids
Reference 01891/15

Lot Recall of Oxoid Antimicrobial Testing Disc, CT0024B CN10 Gentamicin, Thermo Fisher Scientific Microbiology Basingstoke PDF, 71KB, File does not meet accessibility standards Date: 14. April 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 01998/15

Recall of Blood Line Systems (Single-Needle) for dialysis machines, Serumwerk Bernburg Vertriebs GmbH PDF, 338KB, File does not meet accessibility standards Date: 14. April 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 01052/15

Safety Notice for the NobelReplace and Replace Select Tapered Implant System, Nobel Biocare PDF, 218KB, File does not meet accessibility standards Date: 14. April 2015 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 01745/15

Corrective action for the Juno DRF System, Philips Medical Systems PDF, 125KB, File does not meet accessibility standards Date: 14. April 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 02021/15