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Corrective Action for Galileo Echo, Immucor PDF, 186KB, File does not meet accessibility standards Date: 22. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04378/09

Information for the monitor units Eclipse™, Varian PDF, 171KB, File does not meet accessibility standards Date: 22. December 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04623/09

Information for the Digital Image Capture System SDC HD 0240050888 and 0240050888i, Stryker PDF, 322KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04714/09

Information for TriniCHECK Control Level 3, Trinity Biotech PDF, 92KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04484/09

Recall of Male Swab, Roche PDF, 15KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04339/09

Information for the automated external defibrillators HeartStart HS1 and HeartStart FRx, Philips PDF, 223KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04499/09

Information for Elecsys Thyroglobulin, Roche Diagnostics PDF, 53KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04152/09

Safety information for Twist Drill, Biomet Microfixation PDF, 78KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 04578/09

Field Safety Notice for Navigation Headset Operator's Manual, GE Healthcare PDF, 71KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04641/09

Information for CelonLab POWER, Celon PDF, 121KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03905/09, 03906/09

Recall of Dimension Vista LOCI Reaction Vessel, Siemens PDF, 46KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04617/09

Field Safety Notice for electrophysiology system Carto 3, Biosense Webster PDF, 118KB, File does not meet accessibility standards Date: 21. December 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04477/09

Recall for Brain Heart Infusion Broth, OXOID PDF, 40KB, File does not meet accessibility standards Date: 16. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04652/09

Recall for Dade Hepzyme, Siemens PDF, 65KB, File does not meet accessibility standards Date: 15. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04422/09

Recall for Sinus Packing, Fuhrmann GmbH PDF, 78KB, File does not meet accessibility standards Date: 15. December 2009 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 04423/09

Safety Notice for HeartStart Vehicle Wall Mount, Philips PDF, 147KB, File does not meet accessibility standards Date: 14. December 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04508/09

Safety Notice for PK7300 Blood Grouping System, Beckmann Coulter PDF, 52KB, File does not meet accessibility standards Date: 14. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04365/09

Safety Notice for AXIOM Iconos R200, Siemens PDF, 56KB, File does not meet accessibility standards Date: 14. December 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03625/09

Corrective action and recall for DELFIA and AutoDELFIA Neonatal-17α-OH-Progesteron-Kits, PerkinElmer PDF, 128KB, File does not meet accessibility standards Date: 14. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04517/09

Corrective Action for Thermo Fisher TCAutomation / enGen Laboratory Automation Systems, Siemens PDF, 28KB, File does not meet accessibility standards Date: 14. December 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04496/09