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Safety Notice for the application of Test Stimulator, Model 3625, Medtronic Inc. PDF, 103KB, File does not meet accessibility standards Date: 30. July 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 03900/13

Corrective action for ETI ANA/ENA 8 Profile, Dr. Fenning Biomed PDF, 216KB, File does not meet accessibility standards Date: 30. July 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 04271/13

Corrective action for ETI dsDNA, Dr. Fenning Biomed PDF, 369KB, File does not meet accessibility standards Date: 29. July 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 04262/13, 04265/13

Corrective action for Serotonin by HPLC Calibrator Set, Biorad PDF, 79KB, File does not meet accessibility standards Date: 29. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03947/13

Safety Notice for the software Keypoint.NET, Alpine bioMed ApS PDF, 430KB, File does not meet accessibility standards Date: 29. July 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 02411/13

Urgent Safety Notice for Paradigm Insulin Infusion Sets, Medtronic PDF, 92KB, File does not meet accessibility standards Date: 26. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 03264/13

Safety Notice for the EZ-IO 45mm 15G Needle Set, Vidacare Corporation PDF, 416KB, File does not meet accessibility standards Date: 26. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 07292/12

Corrective action for recomLine Parvovirus B19 IgM und recomLine Parvovirus B19 IgG, Mikrogen PDF, 36KB, File does not meet accessibility standards Date: 26. July 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 03428/13

Safety Notice for the Transpedicular Schanz Screw, SYNTHES PDF, 594KB, File does not meet accessibility standards Date: 26. July 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 03569/13

Extended Recall for the 1L Receptal Systems, Hospira PDF, 953KB, File does not meet accessibility standards Date: 26. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01916/13

Corrective action for D999 Membrane Box, pO2, for ABL/50/5XX, Radiometer PDF, 20KB, File does not meet accessibility standards Date: 26. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03411/13

Additional Information concerning the corrective action for AMH Gen II Elisa, Beckman Coulter PDF, 88KB, File does not meet accessibility standards Date: 25. July 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 07449/12

Safety Notice for the product Acurate TA™ Transapical Aortic Bioprosthesis, SYMETIS PDF, 836KB, File does not meet accessibility standards Date: 25. July 2013 Type: Customer information

Product group Non-active implants - cardiac surgery
Reference 03427/13

Corrective action for Unyvero Pneumonia Sets, Curetis PDF, 51KB, File does not meet accessibility standards Date: 25. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03912/13

Lot Recall for the Stryker T4/T5 Hytrel Toga, Stryker PDF, 135KB, File does not meet accessibility standards Date: 25. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03159/13

Chargenrückruf für OP-Bekleidung Stryker T4 / T5 Hytrel-Toga, Stryker PDF, 133KB, File does not meet accessibility standards Date: 25. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03159/13

Recall for the QuickDraw™ Venous Cannula, Edwards Lifesciences Services GmbH PDF, 67KB, File does not meet accessibility standards Date: 24. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03031/13

Recall for the NAVIX™ Access Devices, Xlumena Inc. PDF, 122KB, File does not meet accessibility standards Date: 24. July 2013 Type: Customer information

Product group Optics / Precision engineering - precision instruments for gastrointestinal and urological endoscopy and hysteroscopy
Reference 02269/13

Corrective action for MMB Calibrator, Siemens PDF, 23KB, File does not meet accessibility standards Date: 24. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03013/13

Lot Recall of the Triathlon Size 3-6 PS Femoral & Tibial Trialing Lower Tray, Stryker PDF, 144KB, File does not meet accessibility standards Date: 24. July 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03851/13