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Recall for POSEY BIOTHANE RESTRAINTS 2900, Posey Company PDF, 104KB, File does not meet accessibility standards Date: 11. March 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 01052/13

Safety notice regarding HBS2 mini screws, GEBRUEDER MARTIN GmbH PDF, 231KB, File does not meet accessibility standards Date: 08. March 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 05205/12

Recall of BiCision instruments (Reference numbers 20195-310, 20195-311 und 20195-312), ERBE Elektromedizin PDF, 242KB, File does not meet accessibility standards Date: 08. March 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 00568/13

Recall IH-Com kit Fullversion, Bio-Rad PDF, 2MB, File does not meet accessibility standards Date: 07. March 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 07616/12

FSN for the insert-augments of the CombiCup R System, Waldemar Link PDF, 278KB, File does not meet accessibility standards Date: 07. March 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05304/12

Extension of the IFU of the product Gallengang- und Pankreasprothesen aus Kunststoff, Mandel & Rupp Medizintechnik GmbH PDF, 58KB, File does not meet accessibility standards Date: 07. March 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 00352/13

Field Safety Notice for Artis Zeego, Siemens PDF, 26KB, File does not meet accessibility standards Date: 07. March 2013 Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 00884/13

Recall of Sysmex CS-2100i / 2000i Systems, Siemens PDF, 36KB, File does not meet accessibility standards Date: 07. March 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00808/13

Corrective action for ADVIA LabCell and WorkCell CDX, Siemens PDF, 35KB, File does not meet accessibility standards Date: 07. March 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00680/13

Corrective Action for STA-Liatest in combination with STA-R / STA-R, Diagnostica Stago PDF, 26KB, File does not meet accessibility standards Date: 05. March 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00322/13

Safety Information for the Dlouhy Carrying Chair Light, DLOUHY GmbH PDF, 962KB, File does not meet accessibility standards Date: 05. March 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 01000/13

Safety Notice / Recall for Hoya One-Piece Intraocular Lenses, Hoya Corp. PDF, 72KB, File does not meet accessibility standards Date: 05. March 2013 Type: Customer information

Product group Non-active implants - special implants
Reference 00699/13

Safety Notice for the Medex® Introducer Set, Smiths Medical International Ltd. PDF, 118KB, File does not meet accessibility standards Date: 05. March 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00902/13

Urgent Safety Notice for IsoSeed and IsoCord, Eckert & Ziegler BEBIG, Berlin PDF, 65KB, File does not meet accessibility standards Date: 04. March 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - implantats emitting radioactive radiation
Reference 07913/12

Corrective Action for Immulite 1000 Third-Generation TSH, Siemens PDF, 34KB, File does not meet accessibility standards Date: 04. March 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00618/13

Lot Recall for the Terumo 50 ml Luer Lock Syringe, Terumo Europe PDF, 148KB, File does not meet accessibility standards Date: 04. March 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 00936/13

Urgent Safety Notice regarding implantable HeartWare Ventricular Assist System (VAS), HeartWare Inc. PDF, 124KB, File does not meet accessibility standards Date: 04. March 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 00883/13

Lot Recall for the DLP Single Stage Venous Cannula with Metal Tip, Medtronic PDF, 82KB, File does not meet accessibility standards Date: 04. March 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00772/13

Safety Notice for the Mizuho OSI 5855 Orthopedic Table Top, Mizuho OSI PDF, 49KB, File does not meet accessibility standards Date: 04. March 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 00448/13

Safety Notice for the Allura Xper FD20 Biplane und Allura Xper FD 20 Biplane OR Table, Philips Healthcare PDF, 829KB, File does not meet accessibility standards Date: 01. March 2013 Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 00664/13