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Recall port systems, Agency for Medical Innovations PDF, 97KB, File does not meet accessibility standards Date: 26. October 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03787/09

Recall for Universal Cables, ConMed Linvatec PDF, 154KB, File does not meet accessibility standards Date: 26. October 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03626/09

Recall for surgical handpieces PowerPro®, PowerProMax™ and Mpower™, ConMed Linvatec PDF, 181KB, File does not meet accessibility standards Date: 26. October 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03614/09

Recall for SKATER Single Step und Choice Lock TCD products, Angiotech-PBN Medicals PDF, 157KB, File does not meet accessibility standards Date: 21. October 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03421/09

Recall for EndoClamp Aortic Catheters, Edwards Lifesciences PDF, 142KB, File does not meet accessibility standards Date: 21. October 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03783/09

Recall for ONLINE TDM Gentamicin Assay, Roche PDF, 58KB, File does not meet accessibility standards Date: 21. October 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03636/09

Recall for Medena tapered suction tips, Astra Tech PDF, 85KB, File does not meet accessibility standards Date: 20. October 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03661/09

Safety Notice for MAMMOMAT Inspiration Biopsy Unit, Siemens PDF, 152KB, File does not meet accessibility standards Date: 20. October 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03635/09

Safety Notice for Allura Integris Systems with OMCP Generator, Philips PDF, 109KB, File does not meet accessibility standards Date: 20. October 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02424/08

Recall for ISKD Intramedullary Skeletal Kinetic Distractor, Orthofix PDF, 241KB, File does not meet accessibility standards Date: 20. October 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03809/09

Safety Notice for Galileo Echo, Immucor PDF, 96KB, File does not meet accessibility standards Date: 19. October 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03528/09

Safety Notice for Radiographic System Floating Tabletop, GE Healthcare PDF, 52KB, File does not meet accessibility standards Date: 19. October 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03416/09

Safety Notice for ImageServer/xd,Sectra Imtec AB PDF, 42KB, File does not meet accessibility standards Date: 19. October 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02974/09

Safety Notice for Natus neoBLUE mini, Natus Medical PDF, 91KB, File does not meet accessibility standards Date: 16. October 2009 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 03605/09

Recall for Endo Femoral Aimers, Smith & Nephew PDF, 41KB, File does not meet accessibility standards Date: 16. October 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03482/09

Lot-recall for RC cementable abutment, Institut Straumann AG PDF, 23KB, File does not meet accessibility standards Date: 15. October 2009 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 03671/09

Safety Notice for HeartStart MRx, Philips PDF, 209KB, File does not meet accessibility standards Date: 15. October 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03732/09

Safety Notice for Prometheus CiCa, Fresenius Medical Care PDF, 96KB, File does not meet accessibility standards Date: 14. October 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03451/09

Recall for Neuron 070 Delivery Catheter, Penumbra Inc. PDF, 222KB, File does not meet accessibility standards Date: 13. October 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03641/09

Recall for Berichrom Heparin, Siemens PDF, 123KB, File does not meet accessibility standards Date: 12. October 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02850/09