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Lot Recall for Intrafix Primeline, B.Braun Melsungen AG PDF, 318KB, File does not meet accessibility standards Date: 21. July 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02205/11

Corrective Action for Biometer Lenstar LS 900, Haag Streit AG PDF, 448KB, File does not meet accessibility standards Date: 21. July 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02952/11

Recall for 24k® Arthroscopy Outflow/Suction Tubing sets, ConMed Linvatec PDF, 86KB, File does not meet accessibility standards Date: 21. July 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03114/11

Recall for the ADVIA Chemistry A1c Calibrator, Siemens PDF, 64KB, File does not meet accessibility standards Date: 20. July 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03006/11

Recall for the DYONICS POWER Synthes Chuck, Smith&Nephew PDF, 36KB, File does not meet accessibility standards Date: 20. July 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02923/11

Safety Notice for Carescape Monitor B850, GE Healthcare PDF, 50KB, File does not meet accessibility standards Date: 20. July 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02467/11

Updated Safety Information for the Trabecular Metal Humeral and Trabecular Metal Reverse Shoulder System, Zimmer PDF, 2MB, File does not meet accessibility standards Date: 20. July 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03342/10

Notification of a change to the Instructions for Use for BacT/ALERT®, bioMérieux PDF, 170KB, File does not meet accessibility standards Date: 20. July 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04674/10

Lot Recall for Foliodrape® protect plus Angiography Set I, Paul Hartmann AG PDF, 16KB, File does not meet accessibility standards Date: 19. July 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02078/11

Safety Notice for the Terumo Advanced Perfusion System 1, Terumo Cardiovascular Systems PDF, 191KB, File does not meet accessibility standards Date: 19. July 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02915/11

Safety Notice for Sequencer used with the LANTIS Oncology Information System, Siemens Healthcare PDF, 44KB, File does not meet accessibility standards Date: 19. July 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03029/11

Lot Recall for the CoreValve Delivery Catheter Systems (DCS), Medtronic PDF, 13KB, File does not meet accessibility standards Date: 19. July 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02019/11

Recall for Neurotrac™MyoPlus2, Verity Medical Ltd. PDF, 116KB, File does not meet accessibility standards Date: 19. July 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02687/11

Safety Notice for Image Diagnost (IDI) MammoWorkstation with a licensed IDI Reporting module, GE Healthcare PDF, 450KB, File does not meet accessibility standards Date: 19. July 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01985/11

Safety Notice for Cirrus™ HD-OCT Models 4000 and 400 with Instrument and Review Software Versions 5.0.0 and 5.1.0, Carl Zeiss Meditec
PDF, 1MB, File does not meet accessibility standards
Date: 18. July 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02222/11

Safety Notice for MOOG Curlin 6000 and PainSmart PDF, 175KB, File does not meet accessibility standards Date: 18. July 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02670/11

Further Recall for Langston Dual-Lumen Pigtail catheters, Vascular Solutions PDF, 209KB, File does not meet accessibility standards Date: 18. July 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02718/11

Lot Recall for CD Horizon Legacy Multi-Axial-Screws and Vertex Cortical Screws, MEDTRONIC PDF, 12KB, File does not meet accessibility standards Date: 15. July 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03045/11

Safety Notice for the Endolite 30mm Pyramid Clamp Adaptors, Blatchford Products Ltd. PDF, 70KB, File does not meet accessibility standards Date: 15. July 2011 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02808/11

Recall for the IGFBP-3 Elisa Reagent Kit, Beckman Coulter PDF, 130KB, File does not meet accessibility standards Date: 15. July 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02388/11

Recall for GEM TEST PT Cartridges, Instrumentation Laboratory PDF, 445KB, File does not meet accessibility standards Date: 15. July 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02950/11

Corrective action for the LeukoSure Enumeration Kit, Beckman Coulter PDF, 94KB, File does not meet accessibility standards Date: 15. July 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02934/11

Safety Notice: Problem with Instrument tables IT01 for Perimeter Octopus 300 and IT02 for Perimeter Octopus 900, Haag-Streit International PDF, 2MB, File does not meet accessibility standards Date: 14. July 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02170/11

Recall for the Solus Anterior Lumbar Interbody Fusion Spinal Spacer System, ALPHATEC SPINE PDF, 45KB, File does not meet accessibility standards Date: 14. July 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02615/11

Safety Notice for the Propaq LT Patient Monitor, Welch Allyn PDF, 699KB, File does not meet accessibility standards Date: 14. July 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02645/11

Recall for Accu-Chek Inform II meters, Roche PDF, 71KB, File does not meet accessibility standards Date: 14. July 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00656/11

Safety Notice concerning implementing a colour code for all thermosept / thermodent canisters, Schülke & Mayr GmbH PDF, 543KB, File does not meet accessibility standards Date: 14. July 2011 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02561/11

Safety Notice for the Optical Guidance Platform (OPG) Software, Varian medical systems PDF, 50KB, File does not meet accessibility standards Date: 14. July 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02901/11

Safety Notice for MX8000Dual v. Exp., Philips PDF, 117KB, File does not meet accessibility standards Date: 13. July 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02981/11

Recall for Anti-Leb (Murine Monoclonal) Blood Grouping Reagent, Immucor PDF, 77KB, File does not meet accessibility standards Date: 13. July 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02842/11