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Corrective action for ABX DIFFTROL, Axon Lab AG PDF, 1MB, File does not meet accessibility standards Date: 19. March 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 01094/13

Lot Recall for the Triathlon Baseplate Impactor/Extractor, Stryker Orthopaedics PDF, 215KB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 01276/13

Recall of two additional lots of Coseal Surgical Sealant, Baxter PDF, 209KB, File does not meet accessibility standards Date: 18. March 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00033/13

Recall of one lot of the Dilatator, De Bakey, Gebrüder Martin GmbH PDF, 211KB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group Medical instruments for use in humans - vascular surgery
Reference 01118/13

Recall for Legionella Test Kit, Thermo Fisher PDF, 22KB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00953/13

Safety Corrective Action for Artis systems with the software Artis VC20x/VC21A/VD10x that have a DSA license installed, Siemens Healthcare PDF, 769KB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 01089/13

Lot Recall for the RimCup Shells, Biomet Spain Orthopaedics S.L. PDF, 3MB, File does not meet accessibility standards Date: 18. March 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 00622/13

Safety Notice for the application of DBS Lead Cups for implantable Deep Brain Stimulation Leads, Medtronic PDF, 173KB, File does not meet accessibility standards Date: 15. March 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 00665/13

Safety Corrective Action regarding the programmer Q-TECH Model 2020 and the subcutaneous defibrillator SQ-RX Model 1010, CAMERON HEALTH/BOSTON SCIENTIFIC PDF, 139KB, File does not meet accessibility standards Date: 15. March 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - defibrillators
Reference 01070/13

Safety Notice for the syngo.plaza SW version VA 20 with Mammography license, Siemens Healthcare PDF, 1MB, File does not meet accessibility standards Date: 15. March 2013 Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 01011/13