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Lot recall of Scotchcast Wet or Dry Cast Padding, 3M Medica PDF, 28KB, File does not meet accessibility standards Date: 23. August 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - dressings
Reference 04773/13

Safety notice regarding HydroSet Injectable HA Bone Substitute, STRYKER PDF, 183KB, File does not meet accessibility standards Date: 22. August 2013 Type: Customer information

Product group Non-active implants - materials for implants
Reference 04404/13

Corrective action for Dimension Vista Systems RF Flex Reagent Cartridges, Siemens PDF, 54KB, File does not meet accessibility standards Date: 22. August 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 04135/13

Recall for Polarizers, Carl Zeiss PDF, 80KB, File does not meet accessibility standards Date: 21. August 2013 Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 02878/13

Information concerning change of expiration date, Johnson & Johnson PDF, 65KB, File does not meet accessibility standards Date: 21. August 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 04294/13

Lot recall of cardiotomy / autotransfusion reservoirs, Maquet Cardiopulmonary AG PDF, 33KB, File does not meet accessibility standards Date: 21. August 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - transfusion kits
Reference 01503/13

Lot recall of Expandable Introducer Sheath Set, Edwards Lifesciences PDF, 38KB, File does not meet accessibility standards Date: 21. August 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 01101/13

Corrective action for Calcium CPC FS, Diasys PDF, 52KB, File does not meet accessibility standards Date: 20. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04842/13

Lot recall of dialysis blood tubing system, B.Braun Avitum AG PDF, 48KB, File does not meet accessibility standards Date: 20. August 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 02107/13

Corrective action for HLA Fusion-Software due to conversion error, One Lambda PDF, 404KB, File does not meet accessibility standards Date: 19. August 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 04782/13