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Corrective action for the Panbio Dengue IgM Capture Elisa, Alere PDF, 92KB, File does not meet accessibility standards Date: 19. June 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 02540/13

Urgent Safety Notice regarding implantable HeartWare® VAS, HeartWare Inc. PDF, 136KB, File does not meet accessibility standards Date: 19. June 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 03243/13

Safety Notice for the products Brilliance 64, Ingenuity Core and Ingenuity Core128, Philips Healthcare PDF, 198KB, File does not meet accessibility standards Date: 18. June 2013 Type: Customer information

Product group Radiological technology - CT scanners
Reference 02677/13

Urgent Safety Notice for Consulta® CRT-P and Syncra® CRT-P devices, Medtronic PDF, 29KB, File does not meet accessibility standards Date: 18. June 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - cardiac pacemakers
Reference 03240/13

Expanded Safety Notice for the product Berman Angiography catheter, Arrow International PDF, 145KB, File does not meet accessibility standards Date: 18. June 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00056/13

Corrective action for HbA1c Flex® reagent cartridge, Siemens PDF, 25KB, File does not meet accessibility standards Date: 18. June 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02234/13

Corrective action for Advia LSP Calibrator, Siemens PDF, 24KB, File does not meet accessibility standards Date: 18. June 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02029/13

Recall of Lead Cups used for capping of implantable Deep Brain Stimulation Leads (DBS), Medtronic PDF, 150KB, File does not meet accessibility standards Date: 18. June 2013 Topics: Medical devices Type: Customer information

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

Recall for the Epix® and Direct Drive Laparoscopic Graspers, Applied Medical Resources PDF, 2MB, File does not meet accessibility standards Date: 17. June 2013 Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 02827/13

Recall for Synchron System Lactate reagent, Beckman Coulter PDF, 25KB, File does not meet accessibility standards Date: 17. June 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02555/13