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Lot Recall of the AlboGraft Polyester Vascular Grafts, LeMaitre Vascular PDF, 3MB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Non-active implants
Reference 03398/13

Safety Notice concerning the revision of the Instruction for Use, Zimmer GmbH PDF, 27KB, File does not meet accessibility standards Date: 11. September 2013 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 03179/11

Revised Safety Notice for the product NordiPen®, Novo Nordisk PDF, 1MB, File does not meet accessibility standards Date: 10. September 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - insulin pens and pen cannulas
Reference 03570/13

Recall of all lots of OF-B194 Gas/Water Feeding Valves, Pentax PDF, 35KB, File does not meet accessibility standards Date: 10. September 2013 Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 05021/13

Lot Recall of the Disposable Tube Set for Power Systems, Aesculap AG PDF, 116KB, File does not meet accessibility standards Date: 10. September 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03080/13

Lot Recall for the Vitoss Bioactive Bone Graft Substitute, STRYKER PDF, 65KB, File does not meet accessibility standards Date: 10. September 2013 Type: Customer information

Product group Non-active implants - materials for implants
Reference 04893/13

Updated Safety Notice for the Eon Mini and Eon Mini Charger, St. Jude Medical PDF, 115KB, File does not meet accessibility standards Date: 09. September 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 05251/13

Safety Notice concerning the walking aid Crocodile 3 from R82 A/S PDF, 66KB, File does not meet accessibility standards Date: 09. September 2013 Type: Customer information

Product group Orthopaedic / Rehabilitation technology - daily living aids
Reference 05089/13

Safety Notice concerning the electric drive max2, AAT Alber Antriebstechnik GmbH PDF, 72KB, File does not meet accessibility standards Date: 09. September 2013 Type: Customer information

Product group Orthopaedic / Rehabilitation technology - mobility aids
Reference 03646/13