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Recall for GEHC 1.5 m and 1.8 m Uni-Circuit anesthesia breathing circuits, GE Healthcare PDF, 106KB, File does not meet accessibility standards Date: 07. July 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02096/09

Safety Notice for GE Signa OpenSpeed and Ovation MR Scanner, GE Healthcare PDF, 47KB, File does not meet accessibility standards Date: 07. July 2009 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 02021/09

Field Safety Notice of the Amplatzer® Cardiac Plug PDF, 57KB, File does not meet accessibility standards Date: 03. July 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01846/09

Recall of all “Action 2000” manual wheelchairs of manufacturer Invacare Aquatec GmbH PDF, 519KB, File does not meet accessibility standards Date: 02. July 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 00689/09

Recall of Powersail Coronary Dilation Catheters PDF, 39KB, File does not meet accessibility standards Date: 02. July 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02142/09

Recall of the hip belt supplied with the products Mobile Advance Seat, Contoured Advanced Seat, Squiggles Early Sitting System and Squiggles Saddle Seat PDF, 625KB, File does not meet accessibility standards Date: 01. July 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01185/09

Recall of actuators for care beds Casa Med II, Casa Vario T and Casa Comfort II PDF, 64KB, File does not meet accessibility standards Date: 01. July 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01933/09

Lot-recall regarding Sorbit-MacConkey-Agar with MUG PDF, 332KB, File does not meet accessibility standards Date: 01. July 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02105/09

Recall Fogarty occlusion catheters, Edwards Lifesciences PDF, 284KB, File does not meet accessibility standards Date: 30. June 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00425/09

Information about iron (rust) contamination of DI Water in ADVIA® LabCell® System Tubing, Siemens Healthcare Diagnostics PDF, 26KB, File does not meet accessibility standards Date: 30. June 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01940/09

Notice of Correction concerning Triage® TOX Drug Screen kits, Biosite Incorporated PDF, 143KB, File does not meet accessibility standards Date: 29. June 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01967/09

Field Safety Notice for dialysis systems Gambro AK 200 S equipped with UFD and AK 200 ULTRA S in combination with BiCart Select, Gambro PDF, 66KB, File does not meet accessibility standards Date: 29. June 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01956/09

DePuy extends the recall of its PFC Sigma femoral System PDF, 273KB, File does not meet accessibility standards Date: 29. June 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01593/09

Recall of DYONICS 25 Tube Sets, Smith & Nephew PDF, 68KB, File does not meet accessibility standards Date: 29. June 2009 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 02112/09

Field Safety Notice of X-ray systems Allura XPER FD10 F/C, FD10/10, FD20/10 and FD20 PDF, 34KB, File does not meet accessibility standards Date: 26. June 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01874/09

Recall of 034.055va T-sleeves Lot R9483 PDF, 102KB, File does not meet accessibility standards Date: 26. June 2009 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 02000/09

Field Safety Notice of the haemofiltration apparatus BM25 PDF, 205KB, File does not meet accessibility standards Date: 26. June 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01949/09

Information that there is a non conformity of the products TriniCAL, TriniCHECK Control Level 1, Level 2, Level 3, Trinity Biotech PDF, 123KB, File does not meet accessibility standards Date: 26. June 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01799/09

Field Safety Notice concerning corrective actions on Explorer and Discovery X-ray Bone Densitometer Systems, Hologic PDF, 185KB, File does not meet accessibility standards Date: 26. June 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01454/09