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Safety Notice for the SynchroMed® implantable infusion pump, Medtronic PDF, 69KB, File does not meet accessibility standards Date: 15. July 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - drug pumps
Reference 03038/13

Lot Recall for the GamCath Short-term Catheters and Vessel Dilators, Gambro PDF, 102KB, File does not meet accessibility standards Date: 15. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03885/13

Recall of the BD Vascutainer ® Flashback Blood Collection needle, Becton Dickinson GmbH PDF, 103KB, File does not meet accessibility standards Date: 15. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 03853/13

Recall for the Sutureless Connector (SC) Intrathecal Catheter, Medtronic Inc. PDF, 52KB, File does not meet accessibility standards Date: 12. July 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - drug pumps
Reference 03110/13

Recall of urological occlusion catheters, hydraulic ureter dilatators, and hydraulic urethral dilators, Teleflex Medical GmbH PDF, 112KB, File does not meet accessibility standards Date: 12. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 02609/13

Recall for the CODMAN® CERTAS™ Programmable Valves, Johnson & Johnson Medical Ltd. PDF, 118KB, File does not meet accessibility standards Date: 12. July 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 02820/13

Recall of Foliodrape Combi Sets, Hartmann AG PDF, 234KB, File does not meet accessibility standards Date: 12. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02505/13

Corrective action for Reflotron Hemoglobin, Roche PDF, 57KB, File does not meet accessibility standards Date: 11. July 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00475/13

Lot Recall for the ASNIS III Cannulated Screws, STRYKER PDF, 105KB, File does not meet accessibility standards Date: 11. July 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 03753/13

Safety Notice for Alaris® GP, GP Guardrails®, GP Plus & GP Plus Guardrails® Infusion Pumps , CareFusion Switzerland PDF, 41KB, File does not meet accessibility standards Date: 11. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 03112/13

Recall of the rigid Suction Wand model S099, Edwards Lifesciences PDF, 29KB, File does not meet accessibility standards Date: 11. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - drainages and suction systems
Reference 03787/13

Safety Information for the WEBECO-Steam-Sterilizers, Webeco GmbH PDF, 94KB, File does not meet accessibility standards Date: 11. July 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 01883/13

Recall for NexGen® CR Micro Implants and Provisionals, Zimmer PDF, 110KB, File does not meet accessibility standards Date: 10. July 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 03776/13

Updated Safety Notice for Infinia nuclear medicine systems, VG and VG Hawkeye nuclear medicine systems, Helix nuclear medicine systems et al., GE Healthcare PDF, 57KB, File does not meet accessibility standards Date: 10. July 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 03482/13

Recall for the Sysmex® CS-2000i Systems, Sysmex PDF, 562KB, File does not meet accessibility standards Date: 09. July 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 02708/13

Recall for Advia Chemistry Total Protein_2 (Urine) (UPRO_2), Siemens PDF, 36KB, File does not meet accessibility standards Date: 09. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02941/13

Safety Notice concerning the PET VCAR application software, GE Healthcare PDF, 151KB, File does not meet accessibility standards Date: 09. July 2013 Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 03124/13

Safety Notice for the Brainlab iPlan, Brainlab AG PDF, 346KB, File does not meet accessibility standards Date: 09. July 2013 Type: Customer information

Product group Radiological technology - navigation systems
Reference 03754/13

Expanded Recall concerning laryngoscope handles manufactured by M. A. Arain & Brothers, Teleflex Medical PDF, 316KB, File does not meet accessibility standards Date: 09. July 2013 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 01455/13

Corrective action of the HeartStart MRx Monitor/Defibrillator, Philips Healthcare PDF, 51KB, File does not meet accessibility standards Date: 09. July 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 03632/13