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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

Field Safety Notice of The ProcedurePak “Oberbauch Set 1715189-05” PDF, 26KB, File does not meet accessibility standards Date: 25. June 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01602/09

Information about an exchange of ABL 77 Cal Packs PDF, 24KB, File does not meet accessibility standards Date: 25. June 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01905/09

Field Safety Notice of the compressor nebulizers MicroElite Standard and MicroElite Deluxe PDF, 31KB, File does not meet accessibility standards Date: 25. June 2009 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 01812/09

Information about the recall of the Eva450EE mobile hoist, serial no 373317696102195 – 373317696102318, RoMedic AB PDF, 154KB, File does not meet accessibility standards Date: 23. June 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01753/09

Information regarding VITROS® 5600 Integrated System because of a software anomaly, Ortho Clinical Diagnostics PDF, 179KB, File does not meet accessibility standards Date: 23. June 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01934/09

Field Safety Notice of the N-DISVENT-02 interface PDF, 1MB, File does not meet accessibility standards Date: 23. June 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01855/09

Recall of different Lots of iUni® Knee Repair Systems PDF, 126KB, File does not meet accessibility standards Date: 23. June 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01510/09

The manufacturer The Surgical Company informs of the warming cassette of a Fluido TA 500 Standard Set PDF, 1MB, File does not meet accessibility standards Date: 23. June 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01088/09

Information regarding incorrect labelling of the electropalatograph-system WinEPG / PTU, Articulate Instruments PDF, 191KB, File does not meet accessibility standards Date: 19. June 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01966/09

Zimmer TMT recalls all TM-400 Broach Handles PDF, 30KB, File does not meet accessibility standards Date: 19. June 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01626/09

Field Safety Corrective Action of Orthofix Srl, Italy, for Prefix – Multi Screw Clamp PDF, 2MB, File does not meet accessibility standards Date: 19. June 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01910/09

Recall of one lot of femoral Modular Neck System, DJO Surgical (formerly Encore Medical) PDF, 67KB, File does not meet accessibility standards Date: 19. June 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00984/09

Recall of affected lots of the coronay stent “Cypher Select ™+“, Cordis PDF, 185KB, File does not meet accessibility standards Date: 19. June 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01596/09

Recall of several lots of Plus SL Standard Stems, Smith & Nephew PDF, 49KB, File does not meet accessibility standards Date: 19. June 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01731/09

Field Safety Notice of Triathlon TS Knee System Offset Adapter Trial PDF, 61KB, File does not meet accessibility standards Date: 19. June 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01699/09