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Boston Scientific recalls Stainless Steel Greenfield™ Vena Cava Filter PDF, 783KB, Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03189/05

Customer Information concerning the surgical lights Admeco-Lux PDF, 45KB, Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03051/05

Recall of the product Removable T-Handle PDF, 42KB, Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02884/05

Terumo Cardiovascular Systems recalls the Sarns Soft Flow Aortic Cannulae with Suture Flange PDF, 133KB, Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02707/05

Becton Dickinson recalls several lot numbers of the peridural anaesthesia products PDF, 147KB, File does not meet accessibility standards Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03139/05

Corrective action and recall of Dade Behring for the BEP 2000 and the BEP 2000 Advance System PDF, 76KB, Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03099/05

Baxter recalls the Intercept BC Platelet Pooling Set and Buffy Coat Pooling Set PDF, 136KB, Date: 29. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03042/05

Safety risk with the BINGO mobility base from Hoggi PDF, 28KB, Date: 22. December 2005 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 03002/05

Potential therapy failure of Sigma pacemakers from Medtronic PDF, 23KB, Date: 22. December 2005 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02984/05

OrbusNeich recalls the SafeCut Coronary Dilatation Catheter PDF, 237KB, Date: 22. December 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02979/05