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Lot Recall for the product Intermed Desinfektionsschaum, ISG Intermed Service GmbH & Co. KG PDF, 854KB, File does not meet accessibility standards Date: 20. September 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 05012/13

Corrective action for Hb 201 microcuvettes, Hemocue PDF, 166KB, File does not meet accessibility standards Date: 20. September 2013 Type: Customer information

Product group In-vitro diagnostics
Reference 04606/13

Urgent Safety Notice for the electrically heated Getinge 46 Series Washer Disinfector with PACS 300, Getinge Group PDF, 3MB, File does not meet accessibility standards Date: 20. September 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 04933/13

Urgent Safety Notice for the CardioQ-ODM/CardioQ-ODM+ Monitoring System and accessories, Deltex Medical PDF, 44KB, File does not meet accessibility standards Date: 20. September 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 04712/13

Recall for the Incise Drape, Mölnlycke PDF, 31KB, File does not meet accessibility standards Date: 20. September 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03364/13

Recall for the devices HYAcorp H 1000, HYAcorp H-S 500 and HYAcorp L, BioScience PDF, 763KB, File does not meet accessibility standards Date: 19. September 2013 Type: Customer information

Product group Non-active implants
Reference 04808/13

Urgent Safety Notice for the products Discovery MR450, Discovery MR750, and Optima MR450w, GE Healthcare PDF, 473KB, File does not meet accessibility standards Date: 19. September 2013 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 05324/13

Safety Notice for the EasyUpgrade DR X-ray system, Philips Healthcare PDF, 56KB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Radiological technology
Reference 05291/13

Recall for REVISIO S Shells, AQ Implants GmbH PDF, 454KB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Non-active implants
Reference 04778/13

Lot Recall of the dialysis concentrate HC 43-90, Fresenius PDF, 2MB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04337/13

Lot Recall of proVencare accessory “J-tipped safety guidewires“, Fresenius Medical Care PDF, 2MB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04080/13

Safety Notice for the HL 30 pump consoles, Maquet Getinge Group PDF, 653KB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00522/13

Safety Notice for Artis zee systems equipped with a card collimator from a specific lot, Siemens Healthcare PDF, 2MB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Radiological technology
Reference 00460/13

Lot Recall for the product Modus 2.0 Cranial Plate, MEDARTIS PDF, 70KB, File does not meet accessibility standards Date: 17. September 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 04941/13

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