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Recall of Model 7428 Kinetra from the manufacturer Medtronic PDF, 138KB, File does not meet accessibility standards Date: 02. August 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01922/06

Recall for the STA Cephascreen 4 reagent from the manufacturer Roche Date: 31. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02073/06

Recall of special lots of the 8F Bard® Channel Steerable Sheath from the manufacturer Enpath Medical Incorporation PDF, 178KB, File does not meet accessibility standards Date: 31. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02100/06

Recall of intrathecal catheters model 8731 and distal revision kits for intrathecal catheter model 8598 form the manufacturer Medtronic PDF, 82KB, File does not meet accessibility standards Date: 31. July 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02116/06

Recall of the UROVACTM Bladder Evacuator from the manufacturer Boston Scientific Corporation PDF, 896KB, File does not meet accessibility standards Date: 28. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02027/06

Replacement of PEGA® CHARGER power supply devices from Pegasus PDF, 62KB, File does not meet accessibility standards Date: 25. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01612/06

Corrective action for Freelite Serum Free Light Chain Assays of The Binding Site PDF, 77KB, File does not meet accessibility standards Date: 25. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01866/06

Information for the Varian EXACT couch in combination with BrainLAB ExacTrac Robotics PDF, 204KB, File does not meet accessibility standards Date: 25. July 2006 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01730/06

Recall of Vidas CA 15-3 from BioMerieux PDF, 172KB, File does not meet accessibility standards Date: 25. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01823/06