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Safety Notice concerning a corrective action of the equipment cart RIWOmobil, Richard Wolf GmbH PDF, 11MB, File does not meet accessibility standards Date: 28. February 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 00716/14

Corrective action for Vitros® Chemistry Products White Correction Factor Slides, Ortho Clinical Diagnostics PDF, 172KB, File does not meet accessibility standards Date: 26. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00059/14

Safety Notice for the device Clear-Flex bag with Emoluer valve, Baxter PDF, 4MB, File does not meet accessibility standards Date: 26. February 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion kits
Reference 00800/14

Corrective action for Immulite® and Immulite® 1000 Osteocalcin, Siemens PDF, 50KB, File does not meet accessibility standards Date: 26. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00708/14

Corrective action for ABX Pentra ML, Horiba ABX PDF, 1MB, File does not meet accessibility standards Date: 26. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00336/14

Corrective action for Alere Triage® TOX Drug Screen, Alere PDF, 165KB, File does not meet accessibility standards Date: 26. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00588/14

Lot Recall of the Cadisc®-L Lumbar Disc Replacement Device, RANIER Technology Ltd. PDF, 74KB, File does not meet accessibility standards Date: 25. February 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06890/13

Safety Notice for the Odalys Screwholder, Kisco International PDF, 181KB, File does not meet accessibility standards Date: 24. February 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00645/14

Lot Recall of the L-Varlock Cage/trial implantat holder, Kisco International PDF, 333KB, File does not meet accessibility standards Date: 24. February 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00569/14

Recall for the Midface Distractor, Synthes GmbH PDF, 66KB, File does not meet accessibility standards Date: 24. February 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00074/14