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Recall of the products TSV 25 Gauge High-Speed Cutter und TSV 25 Gauge High-Speed Posterior Vitrectomy Pack from Bausch & Lomb PDF, 56KB, File does not meet accessibility standards Date: 05. April 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 00505/07

Corrective actions concerning the OEC UroView 2800 Systems from GE Healthcare PDF, 134KB, File does not meet accessibility standards Date: 05. April 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02784/06

Malfunction in the using of the OR table of the MAGNETOM Espree System from Siemens PDF, 75KB, File does not meet accessibility standards Date: 05. April 2007 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 00831/07

Information concerning the syngo Cardiac Echo Quantification feature in syngo Dynamics version 5.0 from Siemens PDF, 67KB, File does not meet accessibility standards Date: 05. April 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00402/07

Information concerning the ICARE intraocular lense from Corneal PDF, 37KB, File does not meet accessibility standards Date: 05. April 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00841/07

Corrective action for all IMPAX systems from Agfa PDF, 117KB, File does not meet accessibility standards Date: 05. April 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00655/07

Information concerning the MammoDiagnost Systems from Philips PDF, 28KB, File does not meet accessibility standards Date: 05. April 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03794/06

Information about the StarClose Vascular Closure System from Abbott PDF, 177KB, File does not meet accessibility standards Date: 04. April 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02680/06

Recall of Suture Passer from Smith & Nephew PDF, 44KB, File does not meet accessibility standards Date: 04. April 2007 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00913/07

Recall of the intraocular lenses GBR/ Vivarte Myopic and Newlife/Vivarte Presbyopic from Ioltech PDF, 140KB, File does not meet accessibility standards Date: 03. April 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00291/07

Information about the exchange of self-sealing screws at the Performix Pro X-Ray Tube used in several CT scanners from GE Healthcare PDF, 97KB, File does not meet accessibility standards Date: 03. April 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00393/07

Information concerning the OEC 9900 Systems from GE Healtcare PDF, 40KB, File does not meet accessibility standards Date: 03. April 2007 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01020/07

Recall of the lot numbers 118532 and 118532A of Trypsik from Diasorin PDF, 39KB, File does not meet accessibility standards Date: 03. April 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00639/07

Corrective action for the Architect Stat Troponin I from Abbott PDF, 150KB, File does not meet accessibility standards Date: 03. April 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00964/07

Incorrect Instructions for Use with the Model 93600 of the Closed Injectate Delivery Systems from Edwards Lifesciences PDF, 120KB, File does not meet accessibility standards Date: 03. April 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00801/07

Recall of the Ringer DeltaSelect irrigation solutions from Delta Select PDF, 67KB, File does not meet accessibility standards Date: 03. April 2007 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 00738/07

Information concerning the prematurely battery depletion of the Lifepak CR Plus and Lifepak Express defibrillators from Medtronic PDF, 83KB, File does not meet accessibility standards Date: 03. April 2007 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00789/07

Recall of the Carotid Wallstent™ Endoprosthesis with Monorail™ Delivery System from Boston Scientific PDF, 179KB, File does not meet accessibility standards Date: 02. April 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00946/07

Recall of the device Zenith from Cook PDF, 34KB, File does not meet accessibility standards Date: 02. April 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00950/07

Information concerning the Vbeam / Aesthetica, Platinum and Perfecta model laser systems from Candela PDF, 72KB, File does not meet accessibility standards Date: 02. April 2007 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 00316/07