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14,979 results

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Safety Notice for the Product Compass 3.1 and 3.1a, IBA Dosimetry GmbH PDF, 4MB, File does not meet accessibility standards Date: 02. March 2015 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 00696/15

Corrective action for the Sealing Screw Tibia UC, Peter Brehm GmbH PDF, 453KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00940/15

Recall for the GENESIS II non-porous Tibial Baseplate, Smith & Nephew PDF, 77KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00870/15

Urgent Safety Notice for the Edwards Commander Delivery System, Edwards Lifesciences LLC PDF, 82KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00669/15

Corrective action for ADVIA Centaur Systems Progesterone Kits, Siemens Healthcare Diagnostics Inc. PDF, 26KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00462/15

Corrective action for the ADVIA Chemistry Systems Drug Calibrator I, Siemens Healthcare Diagnostics Inc. PDF, 27KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00278/15

Safety Notice for the SD BIOLINE Malaria Ag products containing single-use buffer ampoule, Standard Diagnostics, Inc. PDF, 2MB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 00619/15

Recall for the Stryker System 6 Aseptic Housings, Stryker Instruments PDF, 255KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 00135/15

Corrective action for Siemens Capillary Caps, Siemens Healthcare Diagnostics Inc. PDF, 24KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 00527/15

Urgent Safety Notice for the DuraDiagnost X-Ray system, Philips Healthcare PDF, 82KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 00530/15

Corrective action for various products for inhalation therapy, Teleflex Medical PDF, 499KB, File does not meet accessibility standards Date: 25. February 2015 Topics: Medical devices Type: Customer information

Product group Physical therapy - insufflation technique
Reference 00584/15

Corrective action for the Philips Allura FC, Philips Healthcare PDF, 310KB, File does not meet accessibility standards Date: 25. February 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 00531/15

Corrective action for Troponin I-Check-1 device, VedaLab PDF, 307KB, File does not meet accessibility standards Date: 25. February 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00604/15

Corrective action for the MultiDiagnost Eleva II/TV systems, Philips Healthcare PDF, 29KB, File does not meet accessibility standards Date: 25. February 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 00522/15

Urgent Safety Notice for the Trophy IRIX scissor arm of the Trophy IRIX Intra-oral X-Ray System, Carestream Dental PDF, 60KB, File does not meet accessibility standards Date: 25. February 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for stomatological diagnostics
Reference 07183/14

Safety Notice/Corrective action for Single Limb Circuit for Pneupac® Ventilators with PEEP Valve, Smiths Medical International Ltd. PDF, 332KB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 00131/15

Recall for the Alcon® Small Volume Syringes 200μL Luer-Lok™, Alcon Laboratories (UK) Ltd. PDF, 357KB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 00698/15

Recall for certain Hydrophilic Acrylic Single Use Intraocular Lens system packs, Rayner Intraocular Lenses Limited PDF, 4MB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00216/15

Follow-up Information for the Nanostim™ Leadless Pacemaker & Delivery System Catheter, St. Jude Medical PDF, 22KB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - cardiac pacemakers
Reference 04254/14

Recall for the product Cannulated screw 7.5, aap Implantate AG PDF, 312KB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00231/15

Updated Instructions for Use (IFU) for the Zenith Alpha™ Thoracic Endovascular Graft, Cook Medical PDF, 330KB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00326/15

Important Information for Baxter peritoneal dialysis Transfer sets, Titanium adapters, Disconnect caps and Clamshells PDF, 64KB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 00733/15

Urgent Safety Notice for the LANTIS™ Oncology Information System Server, Siemens AG PDF, 24KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 00279/15

Recall for the products REVISIO MTR Femur- und Tibiastiele, AQ Implants GmbH PDF, 2MB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 08716/14

Corrective action for the ISKD - Intramedullary Skeletal Kinetic Distractor (Limb Lengthener), Orthofix Inc. PDF, 167KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00139/15

Corrective action for the MRI systems with superconducting magnets, GE Healthcare PDF, 118KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 00448/15

Safety Notice for MiniCaps with Povidone-lodine, Baxter PDF, 255KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 00265/15

Urgent Safety Notice for the product Digital Linear Accelerator, Elekta Limited PDF, 268KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 00221/15

Urgent Safety Notice for the ACUSON S2000 Automated Breast Volume Scanner (ABVS), Siemens Medical Solutions USA, Inc. PDF, 6MB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 00089/15

Corrective action for the N Latex IgM, Healthcare Diagnostics PDF, 29KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 08453/14