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14,979 results

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Corrective action for ACL AcuStar System Software, Instrumentation Laboratory PDF, 21KB, File does not meet accessibility standards Date: 28. November 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 05452/13

Recall for TRANSRADIAL ARTERY ACCESS KITS, Arrow International Inc. PDF, 136KB, File does not meet accessibility standards Date: 28. November 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 06094/13

Recall of ADROIT™ 6F Guiding Catheters, Cordis PDF, 69KB, File does not meet accessibility standards Date: 28. November 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 04811/13

Urgent Safety Notice for the Philips Expression Information Portal (IP5), Philips PDF, 125KB, File does not meet accessibility standards Date: 27. November 2013 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 06994/13

Voluntary Recall of Anaconda™-ONE-LOK Bifurcate Body and Anaconda™ Bifurcate Body, VASCUTEK Ltd. PDF, 2MB, File does not meet accessibility standards Date: 27. November 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 06372/13

Recall for OtisMed ShapeMatch Cutting Guides, Stryker PDF, 767KB, File does not meet accessibility standards Date: 27. November 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02082/13

Recall for FreeStyle Lite® test strips, Abbott PDF, 85KB, File does not meet accessibility standards Date: 27. November 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 06883/13

Lot Recall for FMS Duo+ and FMS Solo surgical irrigation tubing sets, DePuy Synthes PDF, 685KB, File does not meet accessibility standards Date: 27. November 2013 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05220/13

Corrective action for HemosIL AcuStar HIT-Ab(PF4-H), Instrumentation Laboratory PDF, 32KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 05493/13

Corrective action for chromID Salmonella Agar, bioMérieux PDF, 219KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 05424/13

Safety Notice for the Ingenuity TF PET/CT Software Version 4.0, Philips Healthcare PDF, 234KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 05414/13

Recall for the VariAx Compression Plates, STRYKER PDF, 539KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05875/13

Safety Notice for the Helical Blade for TFN, SYNTHES PDF, 3MB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05943/13

Safety Notice for Central Monitor CNS-6201 series, Nihon Kohden PDF, 204KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 06846/13

Recall of the Magstim 90mm High Power Coil, Magstim Company Limited PDF, 62KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 05584/13

Urgent Safety Notice for the Application Instrument for Sternal ZipFix™, Synthes GmbH PDF, 73KB, File does not meet accessibility standards Date: 26. November 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05283/13

Corrective action for Advia 1200, 1650, 1800 and 2400 Chemistry Systems, Siemens PDF, 26KB, File does not meet accessibility standards Date: 25. November 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05355/13

Lot Recall of VORTEK® Double Loop Ureteral Stent Open/Open With Connectable Pusher and VORTEK® Hydro-Coated Double Loop Ureteral Stents, Coloplast PDF, 66KB, File does not meet accessibility standards Date: 25. November 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 04072/13

Recall of several dental implants, Biomet 3i PDF, 105KB, File does not meet accessibility standards Date: 25. November 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 05349/13

Urgent Safety Notice for the ADM®/MDM® Ball Impactor Tip and ADM® RIM Impactor Tip Instruments, Stryker PDF, 97KB, File does not meet accessibility standards Date: 25. November 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06067/13