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Inion recalls Inion Hexalon Biodegradable ACL/PCL Screw PDF, 45KB, Date: 30. September 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02356/05

Safety advice for the Modular Plus system from Plus Orthopedics PDF, 77KB, Date: 30. September 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02231/05

Software update of the MAGNETOM Sonata system from Siemens PDF, 85KB, Date: 30. September 2005 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 02346/05

Error in the CustomCornea® software of the LADARVision4000® Excimer Laser System from Alcon PDF, 48KB, Date: 30. September 2005 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02113/05

Plus Orthopedics recalls some lots of TC-Plus Solution Inserts PDF, 147KB, Date: 28. September 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02359/05

Unintentional movements concerning the C-arm of Integris Allura Biplan X-ray Imaging Systems from Philips PDF, 54KB, Date: 27. September 2005 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01751/05

AGA Medical recalls AMPLATZER® Vascular Plug PDF, 85KB, Date: 27. September 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02262/05

Medical Device PDF, 502KB, Date: 27. September 2005 Topics: Medical devices Type: Customer information

Reference 01482/05

Corrective action and recall of Radiometer for capillary adapters for ABL5 blood gas analyzers PDF, 32KB, Date: 27. September 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01189/05

Plus Orthopedics recalls the TC-Plus Solution tibial components PDF, 25KB, Date: 22. September 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02055/05

Plus Orthopedics recalls the TC-Plus Solution tibial components PDF, 26KB, Date: 22. September 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02288/05

Sedana recalls the Instruction for Use PDF, 39KB, Date: 22. September 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01244/05

Medical Device PDF, 65KB, Date: 22. September 2005 Topics: Medical devices Type: Customer information

Reference 01014/05

Medtronic recalls the Lifepak 500 and Lifepak CR Plus PDF, 419KB, Date: 22. September 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01880/05

Recall Urgent Safety Information for COLLEAGUE infusion pumps from Baxter PDF, 109KB, Date: 22. September 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01850/05

Software upgrade concerning the HeartStart MRx from Philips PDF, 205KB, Date: 20. September 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01117/05

Correct use of the secondary locking mechanism of BrainLAB-Couchmount PDF, 101KB, Date: 19. September 2005 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01510/05

Recall of the camera Endocam Controller from Richard Wolf PDF, 944KB, Date: 19. September 2005 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 01851/05

Biosense Webster recalls the Celsius® ThermoCool® and NaviStar® ThermoCool® irrigated ablation catheters PDF, 69KB, Date: 19. September 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02065/05

Corrective action on volumetric infusion pumps Volumed μVP7000 from Arcomed PDF, 77KB, Date: 19. September 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01906/05

Failure of a special population of roller pumps for Arterial pumps from TERUMO PDF, 106KB, Date: 12. September 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00848/05

Issue with the patient table of the MAGNETOM from Siemens PDF, 67KB, Date: 12. September 2005 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 02145/05

Software update of the On-Board Imager from Varian PDF, 115KB, Date: 12. September 2005 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01610/05

Anomaly in CadPlan version 6.4.7 from Varian PDF, 91KB, Date: 12. September 2005 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01607/05

Perouse Laboratoires recalls POLYSHUNT® PDF, 74KB, Date: 12. September 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02161/05

Conterfeits of the Accu-Check Softclix lancets from Roche PDF, 32KB, Date: 12. September 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02172/05

Correction of the LeVeen™ Needle Electrode from Boston Scientific PDF, 179KB, Date: 12. September 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02127/05

Risk with the peritonealdialysis systems HomeChoice and HomeChoice Pro from Baxter PDF, 201KB, Date: 12. September 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01694/05

Curative recalls PorticoPorts PDF, 59KB, Date: 09. September 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02044/05

Angiomed recalls Bard® LUMINEXX® Endoscopic Biliary Stent and Bard® memotherm® Colorectal Stent PDF, 112KB, Date: 09. September 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01954/05