BfArM - Federal Institute for Drugs and Medical Devices

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Urgent Safety Notice for various Pins, Wires and Drill Bits, Smith & Nephew PDF, 121KB, File does not meet accessibility standards Date: 06. July 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02879/11

Safety Notice for the wheelchair Permobil C500 Corpus Lowrider, Permobil PDF, 88KB, File does not meet accessibility standards Date: 06. July 2011 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02935/11

Safety Notice for the MS2 mobile stand, Moor Instruments PDF, 72KB, File does not meet accessibility standards Date: 05. July 2011 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02410/11

Urgent Safety Notice: 2.24 programmer software version and Reply / Esprit pacemakers, Sorin CRM S.r.I. PDF, 71KB, File does not meet accessibility standards Date: 05. July 2011 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01966/11

Recall for Minutex D-Dimer, Tcoag PDF, 98KB, File does not meet accessibility standards Date: 05. July 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02474/11

Recall for GEM Premier 3500, Instrumentation Laboratory PDF, 83KB, File does not meet accessibility standards Date: 05. July 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02494/11

Update to a communicated Recall for the NexGen® Complete Knee Solution Posterior Referencing Instruments, Zimmer Inc. PDF, 306KB, File does not meet accessibility standards Date: 05. July 2011 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01365/11

Safety Notice concerning a corrective action of the Lifepak 500 automated external defibrillator, Medtronic Physio-Control PDF, 72KB, File does not meet accessibility standards Date: 04. July 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02793/11

Recall of certain lots of the Trinity Biolox Delta liner and Corin Biolox Delta modular head, Corin Medical Ltd PDF, 806KB, File does not meet accessibility standards Date: 04. July 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02602/11

Urgent Safety Notice for Varian High Energy Clinacs® and TrueBeam™ Systems, Varian medical systems PDF, 191KB, File does not meet accessibility standards Date: 04. July 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02546/11