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Recall of Becton Dickinson for the BD ProCOUNTTM Progenitor Cell Enumeration Kit PDF, 46KB, Date: 19. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02091/05

Corrective action and recall from Radiometer Medical for ABL700/800 analyzers PDF, 147KB, Date: 19. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01790/05

Recall of the software of the ACL Top system, Instrumentation Laboratory PDF, 95KB, Date: 19. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02064/05

Recall of the software of ACL Futura and ACL Advance systems, Instrumentation Laboratory PDF, 100KB, Date: 19. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02062/05

Recall of Abbott for the software of i-Stat analyzers PDF, 143KB, Date: 19. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01903/05

Boston Scientific recalls Tearaway Introducer (Peelable) Sheaths PDF, 331KB, Date: 19. August 2005 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02016/05

Correct fitting of Distal Covers MAJ-311/411 for duodenoscopes from Olympus PDF, 148KB, Date: 17. August 2005 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 01316/05

LEXXOO International recalls LEXX Tageslinsen PDF, 82KB, Date: 17. August 2005 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 01741/05

Recall of power supplies for FlowScreen flowmeters from Viasys PDF, 56KB, Date: 17. August 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01588/05

Software-Update on the Telemetry Systems WEP-4200 from Nihon Kohden PDF, 86KB, Date: 17. August 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01735/05

Corrective action and recall from for the software of Olympus systems AU400, AQU640 and AU2700 PDF, 37KB, Date: 17. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01682/05

Reduction in nebulizing performance of Nebulizer OMRON MicroAir PDF, 34KB, Date: 12. August 2005 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 02360/04

Guidant recalls Omnilink Peripheral Stent Systems PDF, 89KB, Date: 12. August 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01795/05

Recall of METRxTMMED Procedure Kits from Medtronic PDF, 106KB, Date: 12. August 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01606/05

Chad Therapeutics recalls the Sequoia Oxymatic OM-311 and OM-312 electronic oxygen conservers PDF, 25KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 00935/05

Angiomed recalls Bard® LUMINEXX® 3 Biliary and Vascular Stents and Bard® LUMINEXX® 6 F Vascular Stents PDF, 62KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01867/05

OrbusNeich recalls Constant SDS PDF, 33KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01964/05

Hill-Rom informs about battery failure in the hand control of the mattress system Duo PDF, 79KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01986/05

Ciba Vision recalls the contact lens care product Clerz PDF, 36KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 01764/05

Corrective action of Lifepak 500 AED from Medtronic PDF, 52KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01074/05

Corrective action for the RIA Unconjugated Estriol Kit, Beckman Coulter PDF, 60KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02001/05

Corrective action and recall of Sysmex and Dade Behring for Sysmex CA-1500, CA-7000 and CA-500 instruments PDF, 144KB, Date: 11. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01440/05

Problems with the ViewForum release 3.4L1 from Philips PDF, 43KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01423/05

Miehtke recalls severeal lots of their control reservoir PDF, 66KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01809/05

Fractures of the backrest tubes of the folding wheelchair Action³ from Invacare PDF, 93KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01504/04

Guidant recalls the HEARTSTRING II Aortic Cutters PDF, 101KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Reference 01647/05

Corrective action of Beckman Coulter for Access Immunosystems Unconjucated Estriol Calibrators PDF, 183KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01912/05

Corrective action of Roche for Accu-Chek Active PDF, 62KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01890/05

Corrective action and recall of Cepheid Europe for DX Software Smartcycler PDF, 56KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01948/05

Recall of Mast Diagnostics for the Mast ESßL Set PDF, 35KB, Date: 09. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01916/05