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Information concerning the X-ray systems Allura Xper FD20/10 and FD20 with Smart Mask option from Philips PDF, 38KB, File does not meet accessibility standards Date: 09. October 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02875/07

Recall of Architect Free T3 from Abbott Date: 08. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03475/07

Corrective action of ABL80 from Radiometer PDF, 38KB, File does not meet accessibility standards Date: 08. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01239/07

Corrective action for XE-Series Haematology Analyzers from Sysmex PDF, 30KB, File does not meet accessibility standards Date: 04. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03476/07

Recall of the Cord Clamp Clippers from Unomedical PDF, 74KB, File does not meet accessibility standards Date: 02. October 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01432/07

Information concerning a software discrepancy for use of MOSAIQ from Elekta Limited PDF, 110KB, File does not meet accessibility standards Date: 02. October 2007 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02811/07

Information concerning the HeartStart XL M4735A defibrillators from Philips Medizinsysteme Böblingen PDF, 47KB, File does not meet accessibility standards Date: 02. October 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02402/07

Corrective action of Varian High Energy and Low Energy Clinacs from Varian Medical Systems PDF, 175KB, File does not meet accessibility standards Date: 01. October 2007 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03423/07

Information about a temperature increase of the transducer surface from Toshiba Medical Systems PDF, 91KB, File does not meet accessibility standards Date: 28. September 2007 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 02497/07

Field safety notice concerning the KALIX II flat foot implant from Newdeal PDF, 234KB, File does not meet accessibility standards Date: 28. September 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02770/07

Recall of the HemoCue Glucose 201 RT System from HemoCue PDF, 59KB, File does not meet accessibility standards Date: 26. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03391/07

Corrective action and recall of the Dimension Clinical Chemistry System (software version 7.4SP1) from Dade Behring PDF, 76KB, File does not meet accessibility standards Date: 26. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03386/07

Recall of the Superflex ring strippers of the first generation from Fehling Instruments PDF, 36KB, File does not meet accessibility standards Date: 26. September 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02505/07

Recall of the products TOM PLUG FOR 01-15400/401 from Stryker PDF, 75KB, File does not meet accessibility standards Date: 25. September 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02625/07

Software discrepancy of the Verify and Record systems IMPAC MOSAIQ version 1.20L1-P4 from Elekta Limited Date: 25. September 2007 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03083/07

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

Recall of the 200 ml disposable syringes manufactured by Nemoto Kyorindo PDF, 27KB, File does not meet accessibility standards Date: 14. September 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02253/07

Recall of the Mechanical Heart valves Advantage® from Medtronic PDF, 245KB, File does not meet accessibility standards Date: 14. September 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01763/07

Corrective action of the RD/Hitachi 902/904/911/912, RD Hitachi/917 Modular P and Modular P for the test glucose in haemolysate from Roche PDF, 183KB, File does not meet accessibility standards Date: 13. September 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00323/07