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Corrective action for the Recipient Vacuum Trephine, Network Medical Products PDF, 354KB, File does not meet accessibility standards Date: 29. July 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04300/14

Corrective action for certain care beds from Hermann Bock GmbH / Replacement of MD201 twin drives from limoss GmbH & Co. KG PDF, 195KB, File does not meet accessibility standards Date: 28. July 2014 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 03800/14

Corrective action concerning the ACL TOP Family Coagulation Systems, Instrumentation Laboratory PDF, 45KB, File does not meet accessibility standards Date: 28. July 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 03699/14

Corrective action for the ADVIA Centaur® CP, Siemens PDF, 36KB, File does not meet accessibility standards Date: 28. July 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 03728/14

Safety Notice for the PTFE Ventilation Tubes, Spiggle & Theis Medizintechnik GmbH PDF, 12MB, File does not meet accessibility standards Date: 28. July 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03373/14

Urgent Safety Notice for the E.CAM® Patient Handling System (PHS), Siemens PDF, 483KB, File does not meet accessibility standards Date: 28. July 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 04242/14

Recall for the FOCUS Gesundheit Kinderwunsch-Test, ulti med Products (Deutschland) GmbH PDF, 213KB, File does not meet accessibility standards Date: 28. July 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00830/13

Corrective action for PCs for use with the AU480, AU680, and PK7300 Systems (InoNet – Mayflower PC), Beckman Coulter PDF, 31KB, File does not meet accessibility standards Date: 25. July 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03943/14

Corrective action for the Oxoid Legionella BCYE Growth Supplement, Thermo Fisher Scientific PDF, 24KB, File does not meet accessibility standards Date: 25. July 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03550/14

Urgent Safety Notice for the Application Instrument of Sternal ZipFix™, Synthes GmbH PDF, 387KB, File does not meet accessibility standards Date: 25. July 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04129/14

Recall for hydrogel contact lenses, Wöhlk-Contact-Linsen GmbH PDF, 2MB, File does not meet accessibility standards Date: 25. July 2014 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - contact lenses
Reference 03655/14

Urgent Medical Device Safety Notification for the CODMAN® CERTAS™ Programmable Valves, Medos International SARL / DePuy Synthes Codman Neuro PDF, 147KB, File does not meet accessibility standards Date: 25. July 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 04228/14

Corrective action for TRIGEN INTERTAN Nails, Smith & Nephew PDF, 112KB, File does not meet accessibility standards Date: 23. July 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03680/14

Recall for the RT-PLUS™ Modular Femoral Components due to a packaging issue, Smith & Nephew PDF, 69KB, File does not meet accessibility standards Date: 23. July 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 04164/14

Corrective action for the Ascenda™ Intrathecal Catheters / Revision Kits, Medtronic PDF, 82KB, File does not meet accessibility standards Date: 22. July 2014 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - drug pumps
Reference 04023/14

Urgent Safety Notice for Sorin Heater Cooler Devices, Sorin Group Deutschland GmbH PDF, 796KB, File does not meet accessibility standards Date: 22. July 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04000/14

Recall for the product Dafilon Blue, B. Braun Surgical S.A. PDF, 3MB, File does not meet accessibility standards Date: 22. July 2014 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 04064/14

Corrective action for the products Nail Insertion Sleeve, elastic T2 Tibia SPI Ø8-11 and Nail Insertion Sleeve, elastic T2 Tibia SPI Ø8-13, Stryker Trauma GmbH PDF, 70KB, File does not meet accessibility standards Date: 22. July 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04053/14

Recall for HARTMANN CombiSets containing Ring Basin Liner, PAUL HARTMANN AG PDF, 74KB, File does not meet accessibility standards Date: 21. July 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03361/14

Recall for the Kimberly-Clark Custom Procedure Trays (CPT’s) containing the Microtek Basin Liner, Kimberly-Clark PDF, 570KB, File does not meet accessibility standards Date: 21. July 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03553/14