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Recall of the lot number 754801F of the Flow-Count Fluorospheres from Beckman Coulter PDF, 68KB, File does not meet accessibility standards Date: 13. June 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02036/07

Recall of the Microcuff® Magill endotracheal tube from Kimberly-Clark Health Care PDF, 96KB, File does not meet accessibility standards Date: 13. June 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01751/07

Recall of the Kompaktor from Richard Wolf PDF, 60KB, File does not meet accessibility standards Date: 11. June 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01618/07

Recall of one lot of the Amplatz Goose Neck® Snare Kit Model GN3000 from EV3 PDF, 59KB, File does not meet accessibility standards Date: 11. June 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01944/07

Recall of the NextStent™ Carotid Stents and Monorail™ Delivery Systems from Boston Scientific PDF, 99KB, File does not meet accessibility standards Date: 11. June 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01646/07

Recall of the Gynecare Prolift Pelvic Floor Repair Systems (Outer Product Code: PFRT01) from Ethicon PDF, 46KB, File does not meet accessibility standards Date: 08. June 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01381/07

Recall of the STA Liatest Free Protein S from Roche PDF, 80KB, File does not meet accessibility standards Date: 08. June 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01557/07

Corrective action of Cell-Dyn 1700 (all serial numbers) from Abbott PDF, 101KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01940/07

Recall of the Infant Nasal CPAP Cannulas/Systems from Teleflex Medical, Hudson RCI PDF, 128KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01764/07

Information concerning a possible damage of the sterile packaging from Celon PDF, 29KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01302/07

Recall of different sterile invasive single use devices from ConMed Linvatec PDF, 534KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01607/07

Recall of the m2000 barcode readers from Abbott PDF, 76KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01832/07

Recall of patella components of the Genesis Knee System from Smith & Nephew PDF, 37KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01864/07

Recall of the 3.5 mm 90-S SERFAS Energy Suction Probe from Stryker Europe PDF, 39KB, File does not meet accessibility standards Date: 06. June 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01538/07

Recall of Maverick2™ Monorail™ Balloon Catheters from Boston Scientific International S.A. PDF, 90KB, File does not meet accessibility standards Date: 05. June 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01725/07

Information about CENTRA Active hearing instrument from Siemens Audiologische Technik PDF, 46KB, File does not meet accessibility standards Date: 05. June 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01145/07

Information about HeartState F2+ defibrillator from Philips Medical Systems PDF, 85KB, File does not meet accessibility standards Date: 05. June 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01573/07

Recall of of MX9636 – MEDEX PDS Kids Kit from Smiths Medical International Ltd PDF, 40KB, File does not meet accessibility standards Date: 05. June 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01807/07

Recall of eight lot numbers of the Flexiflo 10 Fr DURA-PEG and one lot of Flexiflo 16 Fr DURA-PEG from Abbott Ireland PDF, 62KB, File does not meet accessibility standards Date: 04. June 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01696/07

Recall of Complete Moisture Plus from AMO Advanced Medical Optics PDF, 71KB, File does not meet accessibility standards Date: 04. June 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 01830/07