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Recall for SynFix-LR Mini-Open Screwdriver, Synthes PDF, 121KB, File does not meet accessibility standards Date: 15. April 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00863/09

Rückruf Burette Sets, Codan PDF, 39KB, File does not meet accessibility standards Date: 15. April 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00919/09

Recall for Burette Set, Codan PDF, 39KB, File does not meet accessibility standards Date: 15. April 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00919/09

Safety Notice for View Point with software version 5.6.6 and 5.6.7, GE Healthcare PDF, 62KB, File does not meet accessibility standards Date: 15. April 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00882/09

Corrective Action for ADVIA 1650 and ADVIA 1800 Chemistry Systems, Siemens PDF, 109KB, File does not meet accessibility standards Date: 09. April 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00888/09

Recall for Genesis II Long Stem, Smith & Nephew PDF, 61KB, File does not meet accessibility standards Date: 09. April 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00311/09

Information for ADVIA Chemistry Systeme, Siemens PDF, 70KB, File does not meet accessibility standards Date: 09. April 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00800/09

Recall of Beckman Coulter for SYCHRON Gentamicin Reagent (GEN) lot M804552 PDF, 417KB, File does not meet accessibility standards Date: 08. April 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00966/09

Safety Notice for CT scanner Brilliance iCT, Philips PDF, 108KB, File does not meet accessibility standards Date: 08. April 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00720/09

Quickels Systems AB has issued an information about a recall regarding certain Decapus II units PDF, 266KB, File does not meet accessibility standards Date: 08. April 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00648/09

Information of the STERRAD® 50 System and STERRAD® NX™ PDF, 98KB, File does not meet accessibility standards Date: 08. April 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 00861/09

Recall for Endobon bloc 12.5 and Endobon bloc 20, Biomet PDF, 67KB, File does not meet accessibility standards Date: 08. April 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00879/09

Recall for HA ABG II and HA DLS Hip Stems, Stryker PDF, 149KB, File does not meet accessibility standards Date: 08. April 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00362/09

Safety Notice for VISIOL® pre-filled syringes, TRB Chemedica PDF, 479KB, File does not meet accessibility standards Date: 08. April 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00292/09

Corrective Action for FC 500 with CXP 2.2 Acquisition Software PDF, 52KB, File does not meet accessibility standards Date: 08. April 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00547/09

Corrective action for software versions VA-15A of ACUSON S2000TM ultrasound systems PDF, 206KB, File does not meet accessibility standards Date: 08. April 2009 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 00631/09

Recall of Swan-Ganz-CCO-Catheters PDF, 299KB, File does not meet accessibility standards Date: 07. April 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00519/09

Mölnlycke Health Care has issued an information about a manufacturing problem regarding ProcedurePak®-Products PDF, 637KB, File does not meet accessibility standards Date: 07. April 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00750/09

Field Safety Notice about a problem when using m3 micro-Multileaf-Collimator (mMLC) PDF, 360KB, File does not meet accessibility standards Date: 07. April 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00846/09

Recall of implantable POLYSITE ports PDF, 2MB, File does not meet accessibility standards Date: 07. April 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00529/09

Information of OneTouch® UltraEasy® System Kits from Lifescan PDF, 58KB, File does not meet accessibility standards Date: 07. April 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00556/09

Information of the correct connection breathing circuit tubes of AS3/ADU Anaesthesia Delivery Units PDF, 2MB, File does not meet accessibility standards Date: 07. April 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00676/09

Safety Notice for AED 10 and MRL Jumpstart defibrillators, WelchAllyn PDF, 2MB, File does not meet accessibility standards Date: 03. April 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00646/09

Information for MEDUMAT Transport, Weinmann PDF, 87KB, File does not meet accessibility standards Date: 02. April 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00533/09

Safety Notice for GEMINI TF 16 and 64 Slice and GEMINI GXL 6 and 16 Slice PET/CT Systems, Philips PDF, 115KB, File does not meet accessibility standards Date: 02. April 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00725/09

Recall of the HEARTSTRING II Proximal Seal System from MAQUET Cardiopulmonary AG PDF, 61KB, File does not meet accessibility standards Date: 02. April 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00582/09

Recall for ARCHITECT Reaction Vessels, Abbott PDF, 41KB, File does not meet accessibility standards Date: 02. April 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04894/08

Field Safety Notice concerning X-ray system Compax 40E from Philips Healthcare PDF, 157KB, File does not meet accessibility standards Date: 02. April 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00782/09

Safety Notice for Sireskop SX and AXIOM Sireskop SD, Siemens PDF, 2MB, File does not meet accessibility standards Date: 02. April 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00447/09

Recall for Easypump ST 100-1, I-Flow PDF, 205KB, File does not meet accessibility standards Date: 01. April 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00823/09