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Recall for Dimension Total Bilirubin (TBIL) Flex reagent cartridge (Lot-Number FC8170) of Dade Behring PDF, 29KB, File does not meet accessibility standards Date: 29. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02987/07

Corrective action and recall for Dimension RxL Max / Xpand Plus Software Version 7.4 und QCC Power Pak of Dade Behring PDF, 25KB, File does not meet accessibility standards Date: 29. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02988/07

Corrective action for Multifibren U on BCS and BCS XP Systems of Dade Behring PDF, 39KB, File does not meet accessibility standards Date: 28. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02287/07

Information about a software update of Acuson Antares and Sonoline Antares ultrasound devices of Siemens PDF, 128KB, File does not meet accessibility standards Date: 28. August 2007 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 02959/07

Corrective action for vancomycin, valproinic acid and tobramycin tests on Cobas C501 and Modular Analytics P analyzers of Roche PDF, 66KB, File does not meet accessibility standards Date: 27. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01423/07

Information concerning an update of the WaveScan WaveFront software to version 3.671 from Advanced Medical Optics, Inc. PDF, 75KB, File does not meet accessibility standards Date: 27. August 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02179/07

Corrective action for the FC 500 with CXP Acquisition Software of Beckman Coulter PDF, 45KB, File does not meet accessibility standards Date: 27. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02936/07

Information concerning the modification of software version 4.29 and the renal replacement therapy device Octo Nova® of the company MeSys GmbH PDF, 108KB, File does not meet accessibility standards Date: 24. August 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02080/07

Recall of electrode belts of the LifeVest-Systems WCD 3000 of ZOLL Lifecor Corporation PDF, 56KB, File does not meet accessibility standards Date: 24. August 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02581/07

Recall for the Dade Actin Activated Cephaloplastin Reagent (Lot-Number 537148) of Dade Behring PDF, 35KB, File does not meet accessibility standards Date: 23. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02874/07

Information concerning possible dysfunction of the auto start mode for bipolar coagulation of Integra LifeSciences PDF, 49KB, File does not meet accessibility standards Date: 23. August 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02348/07

Corrective action of Roche for Stago STA Compact and STA Compact CT analyzers Date: 22. August 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02601/07

Recall of microkeratome devices Zyoptix XP Epi Separator and Zyoptix XP Epi Head of the manufacturer Bausch & Lomb. PDF, 41KB, File does not meet accessibility standards Date: 22. August 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02251/07

Recall of Disposable Twist Drill from Biomet 3i PDF, 40KB, File does not meet accessibility standards Date: 21. August 2007 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 02007/07

Information about the Clinical Information Center (CIC) Pro from GE Healthcare Technologies PDF, 62KB, File does not meet accessibility standards Date: 21. August 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02832/07

Information concerning the recall of laser devices EndoSet and EndoFiber of the company Asclepion Laser Technologies GmbH PDF, 38KB, File does not meet accessibility standards Date: 21. August 2007 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02442/07

Information concerning the BV Pulsera and Endura Release 2 systems of Philips Medizin Systeme GmbH PDF, 29KB, File does not meet accessibility standards Date: 21. August 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02798/07

Recall of specific lot numbers of the IV Fluid Administration and Irrigation Sets for the Level-1-System from Smiths Medical Deutschland PDF, 39KB, File does not meet accessibility standards Date: 21. August 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03092/06

Recall of the products BD Visc Viscoelastic Solution from Becton Dickinson PDF, 129KB, File does not meet accessibility standards Date: 20. August 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02425/07

Information of remote controlled X-ray systems from Philips Medical Systems PDF, 54KB, File does not meet accessibility standards Date: 17. August 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00144/06