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Safety Notice for AXIOM Aristos FX and FX Plus, Siemens Healthcare PDF, 108KB, File does not meet accessibility standards Date: 08. April 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01626/10

Urgent Safety Notice for Alcon Custom Paks / Becton Dickinson´s Microlance 30 G Needles, Alcon Pharma GmbH PDF, 242KB, File does not meet accessibility standards Date: 07. April 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 00985/11

Adisory Notice for the Matrix Spine System, Synthes PDF, 28KB, File does not meet accessibility standards Date: 07. April 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01343/11

Safety Notice for the Lucas 2 Chest Compression System, Medtronic Physio-Control PDF, 24KB, File does not meet accessibility standards Date: 07. April 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00880/11

Sicherheitsinformation / Korrektive Maßnahme für LUCAS 2 Thoraxkompressions-System, Medtronic Physio-Control PDF, 49KB, File does not meet accessibility standards Date: 07. April 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00880/11

Safety Notice for syngo plaza, Siemens Healthcare PDF, 128KB, File does not meet accessibility standards Date: 07. April 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01024/11

Safety Notice for WaveLight EX500 Excimer Laser, Alcon Pharma GmbH PDF, 143KB, File does not meet accessibility standards Date: 07. April 2011 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 01378/11

Recall for ELEKTRA bimaterial screwed cups, Small Bone Innovations International PDF, 70KB, File does not meet accessibility standards Date: 06. April 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04824/10

Safety Information for the use of the Kern Lifter Scales, Kern & Sohn GmbH PDF, 104KB, File does not meet accessibility standards Date: 05. April 2011 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 00951/11

Safety Notice for UniCel® DxH ™ 800 COULTER® Cellular Analysis System, Beckman Coulter PDF, 200KB, File does not meet accessibility standards Date: 05. April 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01134/11

Recall for TeCorp implants, Scient´X PDF, 103KB, File does not meet accessibility standards Date: 05. April 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03978/10

Safety Notice for UniCel® DxH™ 800 systems, Beckman Coulter PDF, 135KB, File does not meet accessibility standards Date: 05. April 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03927/10

Safety Notice for the Terumo Advanced Perfusion System 1: Occluder and Air Bubble Detect Modules, Terumo PDF, 74KB, File does not meet accessibility standards Date: 05. April 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01103/11

Safety Notice for Desktop Pro™ R7.01, Elekta PDF, 94KB, File does not meet accessibility standards Date: 05. April 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 00556/11

Lot Recall for Super Arrow-Flex(R) Percutaneous Sheath Introducer Set with Integral Hemostasis Valve/ Side Port, Teleflex Medical PDF, 37KB, File does not meet accessibility standards Date: 04. April 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01243/11

Lot Recall for "Monoaxial pedicular screws" Odalys, KISCO PDF, 39KB, File does not meet accessibility standards Date: 04. April 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01100/11

Safety Notice for Luxtec® MLX Light Source, Integra PDF, 66KB, File does not meet accessibility standards Date: 04. April 2011 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 01303/11

Recall for PillCam Express Video Capsule Delivery Device, Given Imaging PDF, 84KB, File does not meet accessibility standards Date: 04. April 2011 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 01161/11

Recall of the NexGen® Complete Knee Solution Posterior Referencing Instruments, Zimmer Inc. PDF, 134KB, File does not meet accessibility standards Date: 04. April 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01365/11

Recall for the HbA1c APT reagent, Beckman Coulter PDF, 38KB, File does not meet accessibility standards Date: 01. April 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01104/11

Recall for XLD Medium, Oxoid PDF, 36KB, File does not meet accessibility standards Date: 01. April 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00831/11

Safety Information and Recall for Penumbra Coil 400, PENUMBRA Inc. PDF, 555KB, File does not meet accessibility standards Date: 01. April 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01259/11

Recall for fT3-CTK Kit, DiaSorin PDF, 58KB, File does not meet accessibility standards Date: 01. April 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00977/11

Safety Notice for Advantage Workstation Reporting Tool, GE Healthcare PDF, 39KB, File does not meet accessibility standards Date: 01. April 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01038/11

Lot Recall for Aequalis Fracture Stems, Tornier PDF, 118KB, File does not meet accessibility standards Date: 01. April 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00707/11

Safety Notice for Greenlight II Laryngoscope Handle and Battery Cartridge, GE Healthcare PDF, 71KB, File does not meet accessibility standards Date: 31. March 2011 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 00938/11

Corrective action for the HemoCue Glucose RT system and the Hemocue Glucose 201 DM RT system, HemoCue PDF, 153KB, File does not meet accessibility standards Date: 31. March 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00911/11

Recall for R3 Biolox® Forte Ceramic Liners, Smith & Nephew PDF, 118KB, File does not meet accessibility standards Date: 31. March 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01051/11