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Lot Recall for FreshLook® colors contact lenses, CibaVision PDF, 108KB, File is accessible Date: 30. August 2010 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02797/10

Safety Notice for WaveScan WaveFront Systems and Offline Programming Module (OPM), AMO PDF, 80KB, File is accessible Date: 30. August 2010 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02242/10

Safety Notice for Philips M1657B Water Trap, used on Gas-Modules M1013A IntelliVue G1, M1019A IntelliVue G5 and M1026B/ M1026BT, Philips Healthcare PDF, 111KB, File is accessible Date: 30. August 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01066/10

Safety Notice for Working Master Mix for LightCycler MRSA Advanced Test, Material No. 05352894190, Roche Molecular Diagnostics PDF, 70KB, File is accessible Date: 27. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01997/10

Safety Notice concerning incorrect Expiration Date on MMG-226A, MMG-232A, MMG-526A (Reservoir and Battery Kits) of certain lot numbers, Medtronic PDF, 14KB, File is accessible Date: 27. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01959/10

Information for DI-Series Administration Sets indicated for use with the Level 1® Fast Flow Fluid Warmers, Smiths Medical PDF, 13MB, File is accessible Date: 27. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00164/08

Recall for ORTHOPILOT DISPOS. PASSIVE MARKER STERILE, Aesculap PDF, 49KB, File is accessible Date: 26. August 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02566/10

Recall RSP Glenoid Inserter, Encore Medical PDF, 80KB, File is accessible Date: 26. August 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02665/10

Recall for IMTEC-ANA-LIA, Human PDF, 53KB, File is accessible Date: 26. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02551/10

Safety Notice for Ionized Calcium and Ionized Magnesium Sensors, Nova Biomedical PDF, 42KB, File is accessible Date: 26. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02568/10

Safety Information for Creatinine Kit Vista 1500® System, Siemens PDF, 199KB, File is accessible Date: 26. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02295/10

Recall for TruCore II Biopsy instruments, Medical Device Technologies dba Angiotech PDF, 142KB, File is accessible Date: 26. August 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02400/10

Operator's guide change Orchestra Base Primea Datenmanager, Fresenius Vial PDF, 10KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02056/10

Safety Information regarding COBAS® AmpliPrep/COBAS TaqMan® system using AMPILINK software v3.1x oder 3.2.x, Roche Diagnostics GmbH PDF, 384KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02179/10

Safety Notice concerning specific serial numbers of CT System Brilliance iCT (Heavyweight), Philips PDF, 1MB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02187/10

Recall of LEVO starting with serial number 913..., LEVO AG PDF, 286KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02255/10

Safety Notice for TREVO Retriever, Concentric Medical Inc. PDF, 520KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00452/10

Lot recall of BI-20052 Endothelin ELISA, Biomedica Medizinprodukte GmbH PDF, 141KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02022/10

Safety Notice for External Pulse Generators PACE 203H, PACE 300 and Model 3085, Osypka Medical GmbH PDF, 246KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02185/10

Follow-up information for corrective action for PK7300, Beckman Coulter (Olympus) PDF, 813KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04891/08