BfArM - Federal Institute for Drugs and Medical Devices

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Lot Recall for Corail Hip Cemented Femoral Stem Without Collar, DePuy PDF, 62KB, File is accessible Date: 20. August 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02035/10

Labelling correction of Hallu-C Plate, right, NEWDEAL PDF, 124KB, File does not meet accessibility standards Date: 20. August 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00709/10

Safety Notice for Optical Guidance Platform used for Clinac® or Novalis®TX machines, Varian PDF, 1MB, File is accessible Date: 20. August 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02227/10

Field Safety Notice for Image-Com Software, TomTec Imaging Systems GmbH PDF, 69KB, File is accessible Date: 20. August 2010 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 02733/10

Field Safety Notice for emergency / transport ventilators Oxylog 3000, Dräger PDF, 102KB, File is accessible Date: 20. August 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02833/10

Recall for BBL™ Staphyloslide™ Latex Test Kit, Becton Dickinson PDF, 87KB, File is accessible Date: 19. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02569/10

Recall for LightCycler VZV Qual Kit, Roche PDF, 44KB, File is accessible Date: 19. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02537/10

Lot Recall for Circular Stapler 32mm, Stapleline PDF, 58KB, File is accessible Date: 19. August 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 02704/10

Recall for LightCycler EBV Quant Kit, Roche PDF, 44KB, File is accessible Date: 19. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02536/10

Recall for arterial catheterisation sets with incorrect assembled introducer cannulas, Teleflex Medical PDF, 193KB, File is accessible Date: 19. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02883/10

Safety Notice for Kolibri Navigation Station 2.0, BrainLAB PDF, 114KB, File is accessible Date: 19. August 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02235/10

Recall for NycoCard U-Albumin, Axis-Shield PoC PDF, 119KB, File is accessible Date: 19. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02309/10

Corrective Action for Access HAV Ab Kit for use on Access Immunoassay Systems, Beckman Coulter PDF, 114KB, File is accessible Date: 18. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01834/10

Recall of End Screw Extender Sleeves, model 1165-10, Zimmer Spine PDF, 41KB, File is accessible Date: 18. August 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01857/10

Safety Information for LiRASTM for Infectious Diseases, Innogenetics PDF, 48KB, File is accessible Date: 18. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02230/10

Recall for Hydromax, Carl Zeiss Meditec PDF, 53KB, File is accessible Date: 18. August 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02508/10

Safety Notice for Apheresis Bowl 0625B-00, Haemonetics PDF, 83KB, File is accessible Date: 18. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02514/10

Recall for New NBP cuffs neo, Dräger PDF, 458KB, File is accessible Date: 18. August 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02250/10

Recall of OIC Peek Cage, OIC Peek Spacer, AVS Peek Spacer, Solis Peek Cage, Stryker PDF, 22KB, File is accessible Date: 17. August 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01952/10

Safety Notice for Shark-2334-Footrest, Sunrise Medical PDF, 284KB, File is accessible Date: 17. August 2010 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02318/10