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Recall of Cordis 6 French Infiniti Selective Diagnostic Catheters PDF, 88KB, File does not meet accessibility standards Date: 24. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01992/06

Recall of the Boston Scientific IQ Guide Wire PDF, 133KB, File does not meet accessibility standards Date: 24. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01993/06

Recall of Expo™ und Impulse™ Angiographic Catheters from Boston Scientific PDF, 287KB, File does not meet accessibility standards Date: 24. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02026/06

Recall of Omnitest plus Control control solution from Braun Melsungen PDF, 39KB, File does not meet accessibility standards Date: 21. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01296/06

Corrective action and recall of for the Advia 2110 Hematology System from Bayer Healthcare PDF, 94KB, File does not meet accessibility standards Date: 21. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01658/06

Recall of Carotid Wallstent™ Monorail™ carotid endoprosthesis from Boston Scientific PDF, 2MB, File does not meet accessibility standards Date: 21. July 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01990/06

Warning against condom special offers in the Internet PDF, 134KB, File does not meet accessibility standards Date: 20. July 2006 Topics: Medical devices Type: Customer information

Product group Contraception
Reference 01989/06

Recall of Lp(a) Calibrator from Wako Chemicals PDF, 53KB, File does not meet accessibility standards Date: 19. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01959/06

Recall of POLYSITE® venous access ports by Laboratoires Perouse PDF, 69KB, File does not meet accessibility standards Date: 19. July 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01886/06

Recall of C-Peptide Kits from Laison PDF, 44KB, File does not meet accessibility standards Date: 17. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01626/06