BfArM - Federal Institute for Drugs and Medical Devices

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Recall for Wiseguide Guide Catheter, Boston Scientific PDF, 859KB, File does not meet accessibility standards Date: 15. April 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00945/09

Recall for Hydra „Blue“ Hydrophilic Coated Nitinol Guide Wire, OptiMed PDF, 170KB, File does not meet accessibility standards Date: 15. April 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00904/09

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