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Corrective action for Immulite / Immulite 1000 Total T4, Dade Behring PDF, 111KB, File does not meet accessibility standards Date: 21. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03370/09

Safety Notice for Trident Acetabular System, Stryker PDF, 141KB, File does not meet accessibility standards Date: 21. September 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03122/09

Recall for Alpha-Fit Stem, Corin PDF, 72KB, File does not meet accessibility standards Date: 21. September 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00562/09

Information for Image Diagnost MammoWorkstations, GE Healthcare PDF, 52KB, File does not meet accessibility standards Date: 18. September 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03318/09

Safety Notice for the Xeno wheelchair, Otto Bock PDF, 59KB, File does not meet accessibility standards Date: 18. September 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02927/09

Urgent Recall for Portex Uncuffed Paediatric Sized Tracheal Tubes, Smith Medical PDF, 454KB, File does not meet accessibility standards Date: 18. September 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03281/09

Safety Notice for several stretchers, Stryker PDF, 128KB, File does not meet accessibility standards Date: 18. September 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 03162/09

Corrective action for ADVIA Centaur® and ADVIA Centaur® XP, Siemens PDF, 24KB, File does not meet accessibility standards Date: 17. September 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03157/09

Recall for several products because of a packaging error, Angiotech PDF, 556KB, File does not meet accessibility standards Date: 17. September 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03365/09

Recall for PKS SEAL Open Forceps, Gyrus ACMI PDF, 153KB, File does not meet accessibility standards Date: 17. September 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03063/09