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Corrective Action for CSU 803x/603x, Dräger PDF, 961KB, File does not meet accessibility standards Date: 28. August 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04706/13

Lot Recall of the RIGIFLEX™ II Single Use Achalasia Balloon Dilator, Boston Scientific PDF, 34KB, File does not meet accessibility standards Date: 28. August 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03134/13

Recall for the T-Flex Aspheric intraocular lenses, Rayner PDF, 6MB, File does not meet accessibility standards Date: 28. August 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 03197/13

Recall of the Joline Acute Dialysis Catheters, Joline GmbH & Co. KG PDF, 1MB, File does not meet accessibility standards Date: 28. August 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00970/13

Corrective action for cobas b 123 Sensor Cartridge BG/ISE/GLU/LAC, Roche PDF, 144KB, File does not meet accessibility standards Date: 27. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03755/13

Corrective action for GlucoMen LX Sensor test strips, EurimPharm PDF, 100KB, File does not meet accessibility standards Date: 27. August 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03844A/13

Corrective action for Dimension Vista® IRON Flex® reagent cartridge, Siemens PDF, 15KB, File does not meet accessibility standards Date: 27. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06578/12

Corrective action for HemoCue Glucose 201 Microcuvettes, HemoCue PDF, 163KB, File does not meet accessibility standards Date: 27. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03823/13

Lot Recall of the Cordis RADIALSOURCE™ Spring Wire Transradial Access Kit product, Cordis Corporation, Inc. and Greatbatch Medical PDF, 119KB, File does not meet accessibility standards Date: 27. August 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03049/13

Corrective action for Phosphorus Reagent, Abbott PDF, 24KB, File does not meet accessibility standards Date: 27. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04819/13

Corrective action for LIAISON® Control Direct Renin, Diasorin PDF, 575KB, File does not meet accessibility standards Date: 26. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04236/13

Corrective action for AQT 90 FLEX Analyzers, Radiometer PDF, 28KB, File does not meet accessibility standards Date: 26. August 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03940/13

Safety Notice for the Alphafit proximally modified stem, Corin Medical Ltd. PDF, 3MB, File does not meet accessibility standards Date: 26. August 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 03250/13

Safety Notice for the FUJIFILM Gastroscope EG-530UT2, FUJIFILM PDF, 69KB, File does not meet accessibility standards Date: 26. August 2013 Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 04900/13

Urgent Safety Notice concerning the TRACOE twist tracheostomy tube, Tracoe Medical GmbH PDF, 5MB, File does not meet accessibility standards Date: 26. August 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 04142/13

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