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Urgent Safety Notice for Bard® Max-Core® Disposable Core Biopsy Instruments, C. R. Bard GmbH PDF, 134KB, File does not meet accessibility standards Date: 27. April 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - gynaecology
Reference 02324/15

Recall for DHS Connecting Screws, Synthes GmbH PDF, 3MB, File does not meet accessibility standards Date: 27. April 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02317/15

Urgent Safety Notice for the product syngo.mMR General VA30, Siemens AG Healthcare Sector PDF, 2MB, File does not meet accessibility standards Date: 23. April 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 02025/15

Update for the Instructions of Use (IFU) and Clinical Use Information for the Parachute Implant System, CardioKinetix PDF, 1,023KB, File does not meet accessibility standards Date: 23. April 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - cardiac surgery
Reference 00911/15

Urgent Safety Notice for the Revaclear 400 dialyzers, Gambro Dialysatoren GmbH PDF, 2MB, File does not meet accessibility standards Date: 23. April 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 02107/15

Corrective action for the Persona Cemented Tibia Drill Bracket, Zimmer PDF, 114KB, File does not meet accessibility standards Date: 23. April 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02382/15

Lot specific recall of the NexGen CRA/LCCK/RHK 5 mm Distal Femoral Augment, Size F, Zimmer PDF, 75KB, File does not meet accessibility standards Date: 23. April 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 02373/15

Urgent Safety Notice for AVEA® Ventilator All Models, CareFusion Respiratory Systems PDF, 55KB, File does not meet accessibility standards Date: 23. April 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 02367/15

Safety Notice for the syngo Workflow MLR, Siemens AG PDF, 3MB, File does not meet accessibility standards Date: 22. April 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 01994/15

Corrective action for EP-FIT PLUS/MPF Ceramic Insert Deltas, Smith & Nephew, Inc. PDF, 69KB, File does not meet accessibility standards Date: 22. April 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 02271/15

Recall of the Oscillating Saw Attachment for Colibri / Colibri II / Small Electric Drive, DePuy Synthes PDF, 581KB, File does not meet accessibility standards Date: 22. April 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02244/15

Corrective action for the MX 16-slice Computed tomography x-ray system, Philips Healthcare PDF, 158KB, File does not meet accessibility standards Date: 22. April 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 02279/15

Additional Information for the pCO2 Membrane Box (D788) used with ABL700 and ABL800 Series Analyzers, Radiometer GmbH PDF, 16KB, File does not meet accessibility standards Date: 22. April 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03966/13

Recall of ETHICON VICRYL™ Suture, Johnson & Johnson International PDF, 155KB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - surgical sutures, vascular loops etc.
Reference 02152/15

Urgent Safety Notice for Medtronic Neuromodulation DBS system extensions, Medtronic Inc. PDF, 256KB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 02328/15

Corrective action for the ISKD - Intramedullary Skeletal Kinetic Distractor (Limb Lengthener), Orthofix Inc. PDF, 157KB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 01085/15

Recall for the Retrograde Cardioplegia Cannula, ANDOCOR n.v. PDF, 2MB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 02080/15

Corrective action for the Lotus™ Valve System, Boston Scientific PDF, 304KB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - cardiac surgery
Reference 02291/15

Corrective action for the Fem-Flex II Femoral Arterial Cannulae, Edwards Lifesciences Services GmbH/Maquet Cardiopulmonary AG PDF, 100KB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 02265/15

Urgent Safety Notice for the Biosense Webster’s SMARTABLATE™ Generator System manufactured by Stockert GmbH PDF, 136KB, File does not meet accessibility standards Date: 21. April 2015 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 01733/15