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Safety Notice for the product Precision 500D with Dual CRT Video Monitor Suspension, GE Healthcare PDF, 62KB, File does not meet accessibility standards Date: 10. June 2013 Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 02987/13

Urgent Safety Notice concerning Medisize Climatrach HME with silicone valve, Medisize BV PDF, 91KB, File does not meet accessibility standards Date: 10. June 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 02237/13

Safety Information about a design change of a four-fold blood bag system, MacoPharma PDF, 220KB, File does not meet accessibility standards Date: 10. June 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 07517/12

Safety Notice for MAQUETs CARDIOHELP-i Software, Maquet Getinge Group PDF, 1MB, File does not meet accessibility standards Date: 10. June 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 01361/13

Recall for Medex® Custom kits containing BD 300865 Plastipak 50 mL Luer Lock Syringe, Smiths Medical PDF, 3MB, File does not meet accessibility standards Date: 10. June 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 02973/13

Safety Notice for the GE Extremity 1.5T MR Scanners (Optima MR 430s / MSK 1.5 Tesla Extreme), GE Healthcare PDF, 69KB, File does not meet accessibility standards Date: 06. June 2013 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 01656/13

Lot Recall of Vacuette Standard and Safety Blood Collection Sets, Greiner Bio-One GmbH PDF, 182KB, File does not meet accessibility standards Date: 06. June 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 01719/13

Trinity Biotech: Recall for G-6-PDH Control, Normal PDF, 568KB, File does not meet accessibility standards Date: 06. June 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02027/13

Recall for Oxoid Antimicrobial Susceptibility Testing Disc AMP10 Ampicillin, Oxoid PDF, 16KB, File does not meet accessibility standards Date: 06. June 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 01531/13

Lot Recall of the NIM Flex EMG Endotracheal Tube, Medtronic PDF, 28KB, File does not meet accessibility standards Date: 06. June 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 02576/13

Safety Notice concerning a corrective action of the HeartStart MRx Monitor/Defibrillator, Philips Healthcare PDF, 61KB, File does not meet accessibility standards Date: 06. June 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02913/13

Safety Notice for COHERENCE Therapist 2.3, Siemens Healthcare PDF, 39KB, File does not meet accessibility standards Date: 05. June 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 01350/13

Lot Recall for the product Confidence Spinal Cement System Kit, DEPUY PDF, 51KB, File does not meet accessibility standards Date: 05. June 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 02334/13

Recall of Omrix Pressure Regulators, Ethicon Biosurgery PDF, 24KB, File does not meet accessibility standards Date: 05. June 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02634/13

Intuitive Surgical, Inc.: Safety Notice for surgical systems da Vinci S, Si and Si-e PDF, 40KB, File does not meet accessibility standards Date: 05. June 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 02180/13

Recall of specified Intuitive Surgical Bipolar Instruments used with the da Vinci Standard System (IS1200), Intuitive Surgical, Inc. PDF, 146KB, File does not meet accessibility standards Date: 05. June 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02964/13

Recall for the LCP Distal Femoral Plate, SYNTHES PDF, 68KB, File does not meet accessibility standards Date: 04. June 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 02339/13

Corrective Action for the Output plate of the MagNA Pure 96 instrument, Roche PDF, 39KB, File does not meet accessibility standards Date: 04. June 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01685/13

Recall of the iMRI Registration Matrix for GE Headholder of the Cranial Navigation System, Brainlab AG PDF, 139KB, File does not meet accessibility standards Date: 04. June 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02898/13