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Recall of the Dimension clinical chemistry system Total triiodothyronine (T3) Flex reagent cartridge from Dade Behring PDF, 30KB, File does not meet accessibility standards Date: 25. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03300/07

Corrective action for the Dimension Vista System V-Lyte Integrated Multisensor from Dade Behring PDF, 27KB, File does not meet accessibility standards Date: 25. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03299/07

Information concerning the e.motion and Columbus Femural Components from Aesculap PDF, 54KB, File does not meet accessibility standards Date: 24. September 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03327/07

Recall of Arm positioning devices (1001. 44CO/DO/EO/FO) and Elbow support devices (1004. 23CO) from Maquet PDF, 405KB, File does not meet accessibility standards Date: 24. September 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02991/07

Recall of the Universal Sling Bar with the product numbers 3156075, 3156085 and 3156095 from Liko PDF, 56KB, File does not meet accessibility standards Date: 19. September 2007 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02268/07

Recall of the Renegade™ Hi-Flo Microcatheter Kit from Boston Scientific PDF, 104KB, File does not meet accessibility standards Date: 19. September 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03281/07

Corrective action for Vidas C. difficile Toxin A&B from of bioMérieux PDF, 66KB, File does not meet accessibility standards Date: 19. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03278/07

Recall of the AED 20 defibrillators from Welch Allyn PDF, 297KB, File does not meet accessibility standards Date: 19. September 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02985/07

Product Safety Notification concerning the systems Precision Rxi and Precision e from GE Healthcare PDF, 76KB, File does not meet accessibility standards Date: 17. September 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00144/06

Corrective action for Precision Xceed blood glucose monitoring products from Abbott PDF, 365KB, File does not meet accessibility standards Date: 17. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03006/07