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Stryker recalls the Scorpio Total Knee Replacement System PDF, 510KB, Date: 26. August 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02039/05

Plus Orthopedics recalls TC-Plus Solution Inserts PDF, 29KB, Date: 25. August 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02019/05

Medical Device PDF, 291KB, Date: 25. August 2005 Topics: Medical devices Type: Customer information

Reference 02096/05

Corrective action of Abbott for Clinical Chemistry Bilirubin Calibrator PDF, 305KB, Date: 25. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02119/05

Potential of overinfusion with the 6060™ Multi-Therapy Infusion Pump, Baxter PDF, 176KB, Date: 25. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01756/05

Exchange of the remote control in wheelchairs model Neo and Elyps from Bischoff & Bischoff PDF, 60KB, Date: 23. August 2005 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02102/05

Problems with the ADVANTAGE® Prosthetic Heard Valve from Medtronic PDF, 124KB, Date: 23. August 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02014/05

Check of the wheels of the Endoscopy Trolleys from Aesculap PDF, 117KB, Date: 23. August 2005 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 01670/05

Stryker recalls T2 Recon Lag Screws PDF, 61KB, Date: 19. August 2005 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01974/05

Bausch & Lomb recalls Amvisc and Amvisc Plus PDF, 118KB, Date: 19. August 2005 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 01953/05

Zimmer recalls one lot of an implantation instrument for hip endoprothesis PDF, 60KB, Date: 19. August 2005 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01844/05

Sony recalls LCD -monitors PDF, 85KB, Date: 19. August 2005 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00941/05

Corrective action from Agen BioMedical, BioMerieux and Behnk Elektronik for Compact X, Compact XR and Combi Systems PDF, 575KB, Date: 19. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01188/05

Recall of Beckman Coulter for the automated pipetting protocol Dil-AFP PDF, 73KB, Date: 19. August 2005 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02047/05

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