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Recall of one lot of the Dilatator, De Bakey, Gebrüder Martin GmbH PDF, 211KB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group Medical instruments for use in humans - vascular surgery
Reference 01118/13

Recall for Legionella Test Kit, Thermo Fisher PDF, 22KB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00953/13

Safety Corrective Action for Artis systems with the software Artis VC20x/VC21A/VD10x that have a DSA license installed, Siemens Healthcare PDF, 769KB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 01089/13

Lot Recall for the RimCup Shells, Biomet Spain Orthopaedics S.L. PDF, 3MB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 00622/13

Safety Notice for the application of DBS Lead Cups for implantable Deep Brain Stimulation Leads, Medtronic PDF, 173KB, File does not meet accessibility standards Date: 15. March 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 00665/13

Safety Corrective Action regarding the programmer Q-TECH Model 2020 and the subcutaneous defibrillator SQ-RX Model 1010, CAMERON HEALTH/BOSTON SCIENTIFIC PDF, 139KB, File does not meet accessibility standards Date: 15. March 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - defibrillators
Reference 01070/13

Safety Notice for the syngo.plaza SW version VA 20 with Mammography license, Siemens Healthcare PDF, 1MB, File does not meet accessibility standards Date: 15. March 2013 Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 01011/13

Recall for IDM software method for EliA Rheumafactor IgM in Phadia® 2500/ Phadia® 5000 Systems, ThermoFisher PDF, 159KB, File does not meet accessibility standards Date: 15. March 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 00706/13

Extension of the Instructions for Use for the Medacta femoral stem, Medacta International SA PDF, 1MB, File does not meet accessibility standards Date: 15. March 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 01140/13

Safety Notice concerning the patient hoist aks-clino II, aks GmbH PDF, 104KB, File does not meet accessibility standards Date: 15. March 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 01225/13

Recall of single-use insufflation tube set 4170.501, Richard Wolf PDF, 15MB, File does not meet accessibility standards Date: 14. March 2013 Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 00901/13

Corrective Action for Dade Actin FSL, Siemens PDF, 27KB, File does not meet accessibility standards Date: 14. March 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 01018/13

Urgent Safety Notice for the endocavitary SE12-3 transducer, SuperSonic Imagine PDF, 461KB, File does not meet accessibility standards Date: 14. March 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 00661/13

Recall of various sets for surgical procedures containing Neoject Cannulas of the manufacturer Dispomed, Raguse GmbH PDF, 293KB, File does not meet accessibility standards Date: 14. March 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 01045/13

Safety Notice for the MitraClip Valve Repair System, Abbott Vascular Evalve Inc. PDF, 297KB, File does not meet accessibility standards Date: 13. March 2013 Type: Customer information

Product group Non-active implants - cardiac surgery
Reference 00939/13

Recall for the Endo GIA AutoSuture Universal Loading Unit 30mm-2.0mm, Covidien PDF, 86KB, File does not meet accessibility standards Date: 13. March 2013 Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 00628/13

Safety Notice for the O-arm® Imaging System, Medtronic PDF, 44KB, File does not meet accessibility standards Date: 13. March 2013 Type: Customer information

Product group Radiological technology - navigation systems
Reference 00424/13

Recall for EasyGas, Fluoron PDF, 2MB, File does not meet accessibility standards Date: 12. March 2013 Type: Customer information

Product group ophthalmological technology - other medical devices for ophthalmological purposes
Reference 00569/13

Safety Notice for the GenIQ software application, GE Healthcare PDF, 82KB, File does not meet accessibility standards Date: 12. March 2013 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 00559/13

Safety Notice for Level 1® Fast Flow Fluid Warmers and Normoflo® Irrigation Fluid Warmer, Smiths Medical PDF, 174KB, File does not meet accessibility standards Date: 12. March 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 00555/13