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Safety Notice for upcoming safety inspection for Symbia E- or e.cam-system, Siemens Healthcare PDF, 74KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 06686/13

Lot Recall of the NX3 Try-In Gel, KERR PDF, 182KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental material
Reference 05568/13

Safety Notice for the IntelliSpace PACS system, Philips Healthcare PDF, 440KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 06700/13

Safety Notice for Artis biplane system, Siemens Healthcare PDF, 1MB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 07112/13

Safety Notice for ConMed Electrosurgery ALTRUS® Termal Tissue Fusion Handpieces (2 lots), ConMed Corporation PDF, 65KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 06493/13

Safety Notice for “Metal-finish” Lamp Modules on th da Vinci Si (IS3000) System Illuminator, Intuitive Surgical Inc. PDF, 786KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 06390/13

Lot recall of Cannulated Screw 3.5, aap Implantate PDF, 304KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06423/13

Lot-recall IMPRINT II REGULAR BODY VPS, 3M Deutschland GmbH (formerly known as ESPE) PDF, 86KB, File does not meet accessibility standards Date: 12. December 2013 Topics: Medical devices Type: Customer information

Product group Dental products - others
Reference 07191/13

Safety Notice for TACTYS – PIP prosthesis, Stryker Osteosynthesis PDF, 112KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 04426/13

Safety Notice for Precision 500D, Legacy, RFX and SFX X-ray imaging systems, GE Healthcare PDF, 72KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 05814/13

Safety Notice for the NOMEX Multimeter, PTW (Physikalisch-Technische Werkstätten) Freiburg PDF, 57KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 06865/13

Safety Notice for ISE Ref-Valves for AU400, AU640, AU2700 and AU5400 Chemistry Analysers and ISE Ref-Valves for AU480, AU680 and AU5800 Chemistry Analysers, BeckmanCoulter PDF, 65KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05668/13

Recall for the Perfusafe cannulas with Huberschliff, VYGON S.A. PDF, 35KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 06696/13

Safety Notice for bariatric bed Total Care, Hill-Rom PDF, 617KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 06635/13

Safety Notice for the Trinica® ALP-System, Zimmer Inc. PDF, 147KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06329/13

Lot Recall for the Lifeshield, Latex-Free, Non-DEHP, Primary Plumset, Hospira PDF, 699KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 06357/13

Safety Notice for Peregrine Surgical Peeler Forceps, Peregrine Surgical Limited PDF, 159KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - eye surgery
Reference 06127/13

Safety Notice for the REPLY, ESPRIT and FACIL pacemakers, Sorin Group Italia S.r.I. PDF, 39KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - cardiac pacemakers
Reference 06964/13

Corrective action of the intraoral digital imaging plate system DIGORA Optime Type DXR-60, Soredex PaloDEx PDF, 167KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 04617/13

Lot Recall of the product Endobon Xenograft Granules 0,5ml, Biomet 3i/ Biomet France PDF, 101KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05505/13

Safety Notice concerning a corrective action of the external defibrillators Samaritan PDU 400, HeartSine Technologies Ltd. PDF, 173KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 06089/13

Lot Recall of the product Excite F DSC, Ivoclar Vivadent AG PDF, 139KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental material
Reference 05811/13

Safety Notice for C-Series Clinac®, Trilogy®, Trilogy Tx™, Novalis Tx™ and Unique linac, VARIAN medical systems PDF, 31KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 05781/11

Safety Notice for Sengstaken tubes and guidewires, Willy Rüsch PDF, 53KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - probes
Reference 05545/11

Safety Notice for Dimension Vista 500 and Dimension 1500, Siemens PDF, 33KB, File does not meet accessibility standards Date: 11. December 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06293/13

Safety Notice for certain Engström Ventilators and Aespire View, Aisys, and Avance anesthesia machines, GE Healthcare PDF, 78KB, File does not meet accessibility standards Date: 10. December 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 06325/13

Safety Notice for Instructions of Cerament Spine Support, Bonesupport PDF, 41KB, File does not meet accessibility standards Date: 10. December 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 07521/12

Recall of the Irrigation Tube Sets, DePuy Synthes PDF, 2MB, File does not meet accessibility standards Date: 10. December 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05824/13

Safety Notice for elastomeric infusion pumps INfusor, FOLfusor and Intermate, Baxter PDF, 82KB, File does not meet accessibility standards Date: 10. December 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 05602/13

Recall of the SynReam-Medullary Reamer Head, DePuy Synthes PDF, 907KB, File does not meet accessibility standards Date: 10. December 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06407/13