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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

Extension of the recall of certain lots of the Mach I™ Guide Catheters from Boston Scientific PDF, 304KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02557/07

Recall of the Colorado 2 Locking Nuts from Medtronic PDF, 231KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03170/07

Recall of the resorbable bone screws Calaxo from Smith & Nephew PDF, 40KB, File does not meet accessibility standards Date: 12. September 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03129/07