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Recall Cannon, Cannon II and Edge, Arrow

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02281/08

Arrow international Corp. (Teleflex Medical) recalls all Cannon, Cannon II and Edge implantable hemodialysis catheters from the market produced before July 2007. The catheter tip may separate after implantation of the affected catheters.

Advisory Notice is only available in German language.

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