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Corrective Action for Dimension Vista Systems Software Version 3.4, Siemens PDF, 31KB, File does not meet accessibility standards Date: 17. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06034/11

Failure in XVI, Elekta PDF, 237KB, File does not meet accessibility standards Date: 16. February 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 00356/12

Batch recall of SUSI Instruments because of potential insterility, Aesculap AG PDF, 168KB, File does not meet accessibility standards Date: 16. February 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 00807/12

Safety issue with 4D Planning procedure option of MultiPlan® Treatment Planning System, Accuray PDF, 318KB, File does not meet accessibility standards Date: 15. February 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 00673/12

Error in software catalog number 71070401 for external fixator Spatial Frame, Smith & Nephew Orthopaedics GmbH PDF, 82KB, File does not meet accessibility standards Date: 15. February 2012 Topics: Medical devices Type: Customer information

Product group Medical data processing (software) - others
Reference 00580/12

Software update for Leica M822 F20 and M822 F40 surgical microscopes required, Leica Microsystems PDF, 111KB, File does not meet accessibility standards Date: 15. February 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 00400/12

Potential defect of the AC/draw/return manifold of Trima Accel Disposable Tubing Sets, CaridianBCT PDF, 222KB, File does not meet accessibility standards Date: 15. February 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 00082/12

Potential of wrong patient images when reviewing images on LOGIQ S8 Ultrasound System, GE Healthcare PDF, 58KB, File does not meet accessibility standards Date: 14. February 2012 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 00713/12

Possibility of probe heads on LOGIQ P6 Ultrasound Systems for heating up, GE Healthcare PDF, 50KB, File does not meet accessibility standards Date: 14. February 2012 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 00672/12

Recall of Creatinine PAP FS (Lot No.: 15317) due to deviating results, DiaSys PDF, 66KB, File does not meet accessibility standards Date: 14. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00667/12