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Corrective action for GlucoMen LX Sensor test strips, axicorp Pharma PDF, 244KB, File does not meet accessibility standards Date: 06. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04383/13

Urgent Safety Notice for the SYNERGY® Circulatory Support System, CircuLite PDF, 132KB, File does not meet accessibility standards Date: 02. August 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 04341/13

Lot Recall of the Edwards EndoReturn Arterial Cannula, Edwards Lifesciences PDF, 30KB, File does not meet accessibility standards Date: 02. August 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 04238/13

Batch Recall of the PPM Wound Film and of the PPM Fistula Adapter Set Plus, Phametra GmbH PDF, 137KB, File does not meet accessibility standards Date: 02. August 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - drainages and suction systems
Reference 03523/13

Corrective action for Dimension® Clinical Chemistry Systems Dimension® TACR Assay, Siemens PDF, 25KB, File does not meet accessibility standards Date: 01. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03958/13

Corrective action for Advia 120 Software V.6.2, Siemens PDF, 22KB, File does not meet accessibility standards Date: 01. August 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 03894/13

Corrective action for Low Range Activated Clotting Time (ACT-LR) Cuvettes, International Technidyne Corporation PDF, 2MB, File does not meet accessibility standards Date: 01. August 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 03938/13

Lot Recall of the product cerv-X, Cervical Cage, ulrich GmbH & Co. KG PDF, 55KB, File does not meet accessibility standards Date: 01. August 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 03957/13

Corrective action for Immulite, Immulite 1000, Immulite 2000 and Immulite 2000 XPi PSA, Siemens PDF, 48KB, File does not meet accessibility standards Date: 01. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03834/13

Corrective action of the Digital Linear Accelerators PRIMUS, ONCOR and ARTISTE, Siemens PDF, 24KB, File does not meet accessibility standards Date: 01. August 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 04343/13